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cph:gen
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genmab.wd3.myworkdayjobs.com
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genmab.wd3.myworkdayjobs.com
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Dec 25th, 2022 12:00AM
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Submission Manager, Regulatory Operations
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Open
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DK001 Genmab A/S
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Copenhagen - Havneholmen 25
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DNK
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Nov 25th, 2022 12:00AM
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<p>Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. </p><p></p><p><b><span>The Role</span></b></p><p></p><p>Genmab is looking for a Submission Manager, Regulatory Affairs to be a part of our Global Regulatory Affairs organization. In this role, the candidate will <span>manage Clinical Trial Applications as part of the Oncology therapeutic area team within Global Regulatory Operations. </span></p><p></p><p>The position is based in Copenhagen, Denmark and you will join a global team of colleagues in DK and US. This position reports to Senior Director, Team Lead, Global Regulatory Affairs Operations</p><p><br /><b><span>Responsibilities</span></b></p><ul><li><p>Be responsible for the submission operational management (planning and tracking) and delivery of regulatory submissions at a compound level to support global development and registration, primarily focused on Clinical Trial Applications (CTAs)</p></li><li><p>Create and handle dossier plans/submission packages in line with regulatory strategy, seeking input from regulatory therapeutic areas, functional area representatives, and vital collaborators, while providing guidance to project team members</p></li><li><p>Contribute to decisions that have an impact on the quality and timeliness of moderate to sophisticated Health Authority submissions</p></li><li><p>Make decisions on submission operational strategies for the best project management approach within process/timeline/resource constraints</p></li><li><p>Lead Submission Team meetings to coordinate the preparation and maintenance of regulatory submissions and filings</p></li><li><p>Take a leadership role for the monitoring and efficiency of the submission process and initiate changes within the scope of decision-making authority to minimize inefficiencies and ensure/improve quality</p></li><li><p>Cultivate effective relationships, maintaining open communication with key partners to ensure priority conflicts, resource issues, and deviations from the plan are identified and resolved</p></li><li><p>Develop departmental work practices, process enhancements/improvements, and associated training materials</p></li></ul><p></p><p><b><span>Requirements</span></b></p><ul><li><p>A minimum of a Master’s degree or equivalent and at least 5 years of relevant/related professional experience, preferably within Regulatory</p></li><li><p>In-depth understanding of drug development process and experience with leading clinical trial applications</p></li><li><p>Ability to demonstrate knowledge of regulatory submissions and filings</p></li><li><p>Proficiency in relevant submission-related Health Authority and Industry regulations and guidelines</p></li><li><p>Proficient use of Regulatory Information Systems</p></li><li><p>Fluency in English; other languages may be required depending on assignment</p></li><li><p>Validated project or submission management capabilities</p></li><li><p>Previous experience leading Submission Team meetings to coordinate the preparation and maintenance of submissions and filings</p></li></ul><p></p><p>Moreover, you meet the following personal requirements:</p><ul><li><p>Strong organizational, communication, and time management skills needed to manage multiple ongoing projects simultaneously</p></li><li><p>This position require attention to details and a structured mindset</p></li><li><p>You work independently with an ability to drive projects to successful outcomes</p></li><li><p>You demonstrate robust cross-functional teamwork skills and enjoy working in a global environment</p></li><li><p>You are a highly motivated and self-driven individual who enjoys being challenged</p></li><li><p>You are able to prioritize your work in a fast paced and changing environment</p></li><li><p>You are result- and goal-oriented and committed to contributing to the overall success of Genmab</p></li></ul><p></p><p><span>Genmab will offer the successful application a challenging position, where the right candidate will have the opportunity to work with highly specialised people across functions in an informal, multicultural environment, with an aim to make a difference in the lives of people with cancer.<br /><br />At Genmab, we pride ourselves on our unique culture. We are committed to make a positive impact on the lives of cancer patients. We hypothesize and experiment to seek innovative solutions, no matter the employee’s role; we speak up, empower each other, and embrace change and growth; we respect and celebrate our differences while working as one team. Teamwork and respect are central pillars of Genmab’s culture and we therefore ensure an inclusive, open, and supportive professional work environment across our international locations. Genmab employees work with determination, challenge the status quo and cultivate a growth mindset in everything we do.</span></p><p></p><p><span>We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. </span>No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability or genetic information.</p><p></p><p><span>Genmab A/S is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website: <a href="http://www.genmab.com/privacy/applicants-hr-genmab-a-s/" target="_blank">http://www.genmab.com/privacy/applicants-hr-genmab-a-s/</a></span></p><p></p><p><b><span>Scam alert</span></b></p><p><i>Please be alerted that at the moment a recruitment scam involving Genmab is circulating. The scam involves recruiters on LinkedIn and elsewhere, pretending to be Genmab employees, headhunting candidates, asking for CVs and other personal information. The scam can include asking for payment for interviews or interview preparation. This communication is not coming from Genmab, we encourage people to stay alert and not to respond to these queries.</i></p>
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Dec 24th, 2022 11:17PM
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Dec 24th, 2022 11:17PM
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Genmab A/S
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Health Care
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Pharmaceuticals & Biotechnology
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cph:gen
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genmab.wd3.myworkdayjobs.com
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genmab.wd3.myworkdayjobs.com
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Dec 25th, 2022 12:00AM
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QA Manager, Quality & Compliance System
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Open
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DK001 Genmab A/S
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Copenhagen - Kalvebod Brygge 43
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DNK
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Nov 25th, 2022 12:00AM
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<p>Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. </p><p></p><p><b><span>The Role</span></b></p><p></p><p>The quality area of Genmab is growing and we are looking for a new colleague. QA Quality & Compliance Systems is part of our Global Quality Assurance function, and we work across GxP areas with process and systems meaning this is a great opportunity to develop yourself within GLP, GCP and/or GMP/GDP/IT.</p><p></p><p><span>As QA Manager, Quality & Compliance System,</span> you will therefore work in a multidisciplinary international QA team to ensure compliance to industry standards and <span>regulations and internal procedures. Genmab is using Veeva Vault as our core platform for Quality, Clinical and Regulatory information. </span></p><p></p><p><span>Global QA is the system owner of Veeva and QA Quality & Compliance is the process owner of the Quality Vault. You</span> will have the opportunity to participate in multiple cross functional activities and drive initiatives as relevant within Learning Management, QMS, EDMS, Inspections, Quality Management Review, Outsourced activities just to mention a few. You will be responsible for ensuring that activities <span>are compliant with</span> Good Practice and <span>Genmab’s Pharmaceutical</span> Quality System and you will be an important quality representative supporting any such activities.</p><p></p><p>You have a good knowledge of GxP (GLP/GCP/GMP) and have been working in one or more of these areas. It will also be a benefit if you have previous experience with working with quality systems.</p><p></p><p>The QA Quality & Compliance Systems team at Genmab currently <span>employs 2 people</span> located in Denmark and as a new team member, you will have good opportunity to influence the future way of working for the team. You<span> will report</span> to the Director QA, Quality & Compliance Systems in DK. The Global QA function has a total <span>of 32 </span>employees <span>supporting GLP/GCP/GMP/GDP/IT activities</span> and are represented in Denmark, the Netherlands, the US and Japan. </p><p></p><p><b><span>Responsibilities </span></b></p><p></p><p>The responsibilities of the QA Manager, Quality & Compliance System will include, but not be limited to:</p><ul><li><p>Drive GxP compliance by monitor our quality system and drive/participate in global compliance programs and improvements initiatives</p></li><li><p>Support Quality Management Review process</p></li><li><p>Maintain the internal audit plan</p></li><li><p>SOP review and SOP authoring</p></li><li><p>Super user of Quality Vault</p></li><li><p>Handling and approval of deviations, CAPAs and change controls</p></li><li><p>Member of the Quality Vault Core Team</p></li><li><p>Help ensure one-quality-voice in the organization</p></li><li><p>Secure inspection readiness across sites</p></li></ul><p></p><p><b><span>Requirements</span></b></p><ul><li><p>You hold a relevant degree in a related life <span>science subject at either Bachelor or Master level. Most important experience</span></p></li><li><p><span>You </span><span>have +5 years’ experience from the</span> pharmaceutical industry within GxP and have a drive to work on the compliance and system side</p></li><li><p>Experience working in <span>an EDMS system</span></p></li><li><p>You have excellent communication skills in English, and a <span>collaborative mindset</span></p></li><li><p>As a person you enjoy a fast paced and <span>changing environment</span></p></li><li><p>You are result and goal orientated and committed to contributing to the overall success of Genmab</p></li></ul><p></p><p><span>Genmab will offer the successful application a challenging position, where the right candidate will have the opportunity to work with highly specialised people across functions in an informal, multicultural environment, with an aim to make a difference in the lives of people with cancer.<br /><br />At Genmab, we pride ourselves on our unique culture. We are committed to make a positive impact on the lives of cancer patients. We hypothesize and experiment to seek innovative solutions, no matter the employee’s role; we speak up, empower each other, and embrace change and growth; we respect and celebrate our differences while working as one team. Teamwork and respect are central pillars of Genmab’s culture and we therefore ensure an inclusive, open, and supportive professional work environment across our international locations. Genmab employees work with determination, challenge the status quo and cultivate a growth mindset in everything we do.</span></p><p></p><p><span>We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. </span>No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability or genetic information.</p><p></p><p><span>Genmab A/S is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website: <a href="http://www.genmab.com/privacy/applicants-hr-genmab-a-s/" target="_blank">http://www.genmab.com/privacy/applicants-hr-genmab-a-s/</a></span></p><p></p><p><b><span>Scam alert</span></b></p><p><i>Please be alerted that at the moment a recruitment scam involving Genmab is circulating. The scam involves recruiters on LinkedIn and elsewhere, pretending to be Genmab employees, headhunting candidates, asking for CVs and other personal information. The scam can include asking for payment for interviews or interview preparation. This communication is not coming from Genmab, we encourage people to stay alert and not to respond to these queries.</i></p>
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Dec 24th, 2022 11:17PM
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Dec 24th, 2022 11:17PM
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Genmab A/S
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Health Care
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Pharmaceuticals & Biotechnology
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cph:gen
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genmab.wd3.myworkdayjobs.com
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genmab.wd3.myworkdayjobs.com
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Dec 25th, 2022 12:00AM
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Senior Clinical Trial Associate
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Open
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DK001 Genmab A/S
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Copenhagen - Kalvebod Brygge 43
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DNK
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Nov 25th, 2022 12:00AM
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<p>Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. </p><p></p><p><b><span>The Role</span></b></p><p></p><p>We are looking for an experienced and dedicated Senior Clinical Trial Associate (CTA) to be part of Global Clinical Operations at our Headquarters in Copenhagen.</p><p></p><p>Global Clinical Operations is part of Genmab Clinical Development and is responsible for managing the Genmab clinical cancer trials from early phase trials (FIH) to late stage trials while ensuring processes lives up to regulations and business ethics.</p><p></p><p>The work environment is within a global setting and characterized by people empowerment, new challenges, and devoted and talented colleagues.</p><p></p><p>In this position, you will be responsible for providing assistance to the Clinical Trial Manager on a number of clinical trials in all relevant aspects of trial preparation, trial conduct, documentation, and archiving.</p><p></p><p><b><span>Responsibilities</span></b></p><ul><li><p>Responsible for setting-up, maintaining, reviewing, QC, and file trial related documents in the eTMF system</p></li><li><p>Support ongoing updates of the trial dashboard, trial budget maintenance and development</p></li><li><p>Handle insurances</p></li><li><p>Arrange internal and external meetings, prepare agendas and write minutes, support QC and development of graphical presentations etc.</p></li><li><p>Main driver of sponsor oversight on the eTMF documents twice a year</p></li></ul><p></p><p>Additionally, the role can also involve tasks related to departmental activities such as:</p><ul><li><p>Development of processes, templates, SOPs and WIs</p></li><li><p>Tracking of trial related documents etc.</p></li><li><p>Maintenance of department dossier</p></li><li><p>Development and maintenance of department share point site</p></li><li><p>Training of new employees</p></li><li><p>Support to student workers</p></li></ul><p></p><p><b><span>Requirements</span></b></p><ul><li><p><span>You have a background as Clinical Trial Associate from a similar position or have an education as registered nurse or similar</span></p></li><li><p><span>Preferably you have worked at least 3 years in an administrative position within the Pharmaceutical industry and are experienced in the planning and execution of clinical trials</span></p></li><li><p><span>You are proficient with both written and spoken English</span></p></li><li><p><span>You are highly skilled within MS Office and have flair for using IT systems</span></p></li></ul><p></p><p>Moreover, you meet the following personal requirements:</p><ul><li><p>You are organized and structured with a sense of details</p></li><li><p>You have the ability to work in an environment with many competing priorities</p></li><li><p>You are service minded</p></li><li><p>You are able to work independently as well as in global teams</p></li><li><p>You have a quality mind set and are able to prioritize your work in a fast paced and changing environment</p></li><li><p>You are result- and goal-oriented and committed to contributing to the overall success of Genmab</p></li></ul><p></p><p><span>Genmab will offer the successful application a challenging position, where the right candidate will have the opportunity to work with highly specialised people across functions in an informal, multicultural environment, with an aim to make a difference in the lives of people with cancer.<br /><br />At Genmab, we pride ourselves on our unique culture. We are committed to make a positive impact on the lives of cancer patients. We hypothesize and experiment to seek innovative solutions, no matter the employee’s role; we speak up, empower each other, and embrace change and growth; we respect and celebrate our differences while working as one team. Teamwork and respect are central pillars of Genmab’s culture and we therefore ensure an inclusive, open, and supportive professional work environment across our international locations. Genmab employees work with determination, challenge the status quo and cultivate a growth mindset in everything we do.</span></p><p></p><p><span>We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. </span>No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability or genetic information.</p><p></p><p><span>Please note that if you are applying for a position in the Netherlands; Genmab’s policy for all permanently budgeted hires in this location is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract. </span></p><p></p><p><span>Genmab A/S is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with you application on our website <a href="https://www.genmab.com/privacy" target="_blank">https://www.genmab.com/privacy</a>. </span></p><p></p><p><b><span>Scam alert</span></b></p><p><i>Please be alerted that at the moment a recruitment scam involving Genmab is circulating. The scam involves recruiters on LinkedIn and elsewhere, pretending to be Genmab employees, headhunting candidates, asking for CVs and other personal information. The scam can include asking for payment for interviews or interview preparation. This communication is not coming from Genmab, we encourage people to stay alert and not to respond to these queries.</i></p>
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Dec 24th, 2022 11:17PM
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Dec 24th, 2022 11:17PM
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Genmab A/S
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Health Care
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Pharmaceuticals & Biotechnology
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cph:gen
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genmab.wd3.myworkdayjobs.com
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genmab.wd3.myworkdayjobs.com
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Dec 25th, 2022 12:00AM
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Downstream Processing CMC Specialist
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Open
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DK001 Genmab A/S
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Copenhagen - Havneholmen 25
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DNK
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Nov 25th, 2022 12:00AM
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<p>Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. </p><p></p><p><b>The Role </b><br /><br />The CMC area of Genmab is growing and looking for a Subject Matter Expert (SME) – Downstream processing CMC Specialist (DSP) to join the CMC, Late Stage Manufacturing Development (LSMD) Team.</p><p></p><p>As the DSP SME, you will be part of a highly dedicated and specialized CMC team leading the late stage development activities of Genmab’s proprietary antibody pipeline programs towards marketing approval (BLA/MAA).</p><p></p><p>The SME will work across project teams to support the CMC Project Managers and work closely with other SMEs for e.g. upstream processing, analytical validation and product characterization as well as with relevant SMEs within jointly developed partner programs.</p><p></p><p><b>Responsibilities</b></p><p></p><p>The SME will be responsible for the following:</p><ul><li><p>Late stage Downstream Processing strategies on ongoing projects</p></li><li><p>Defining the scope for the late stage downstream development activities together with our CMO’s and partners according to latest industry standards and regulatory guidance</p></li><li><p>Oversight of DSP manufacturing, characterization, and validation activities performed at partnered CMO’s e.g. trouble shooting, process characterization or process performance qualification</p></li><li><p>Preparation/review of technical documents including development/tech transfer reports, batch records, SOPs</p></li><li><p>Authoring and review of CMC regulatory DSP submissions documents</p></li><li><p>Working closely with upstream processing SME’s to develop late stage development manufacturing process strategies</p></li><li><p>Being the Genmab representative at the CMO during pre-approval inspections for DSP topics</p></li><li><p>Support defining/refining required processes for DSP activities</p></li></ul><p></p><p><b>Requirements</b></p><ul><li><p>It is expected that you have a master’s degree in natural science, pharmacy or similar</p></li><li><p>You have at least 5-10 years of documented professional experience from the CMC area, preferable from late stage development</p></li><li><p>You have a thorough understanding and overview of downstream processes together with an in-depth knowledge of downstream process characterization, risk assessment and validation activities</p></li><li><p>You preferable have active and recent experience within downstream processing development and DOE for biologics/monoclonal antibodies from a phase II/III program</p></li><li><p>It is preferred that you have experience in preparing and reviewing relevant filing documentation for regulatory market authorizations</p></li><li><p>Excellent communication skills in English written and oral</p></li></ul><p></p><p>Moreover, you meet the following professional requirements:</p><ul><li><p>You are focused on achieving goals that are important for the team and our organization</p></li><li><p>You have the ability to work successfully under pressure in a fast-paced environment and with tight timeline</p></li><li><p>You are pro-active, take initiative, and responsibility</p></li><li><p>You are a team player with demonstrated ability to collaborate with a diverse group of internal and external stakeholders</p></li><li><p>With your positive attitude, you enjoy working in multicultural teams inside and outside of Genmab</p></li></ul><p></p><p><span>Genmab will offer the successful application a challenging position, where the right candidate will have the opportunity to work with highly specialised people across functions in an informal, multicultural environment, with an aim to make a difference in the lives of people with cancer.<br /><br />At Genmab, we pride ourselves on our unique culture. We are committed to make a positive impact on the lives of cancer patients. We hypothesize and experiment to seek innovative solutions, no matter the employee’s role; we speak up, empower each other, and embrace change and growth; we respect and celebrate our differences while working as one team. Teamwork and respect are central pillars of Genmab’s culture and we therefore ensure an inclusive, open, and supportive professional work environment across our international locations. Genmab employees work with determination, challenge the status quo and cultivate a growth mindset in everything we do.</span></p><p></p><p><span>We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. </span>No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability or genetic information.</p><p></p><p><span>Genmab A/S is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website: <a href="http://www.genmab.com/privacy/applicants-hr-genmab-a-s/" target="_blank">http://www.genmab.com/privacy/applicants-hr-genmab-a-s/</a></span></p><p></p><p><b><span>Scam alert</span></b></p><p><i>Please be alerted that at the moment a recruitment scam involving Genmab is circulating. The scam involves recruiters on LinkedIn and elsewhere, pretending to be Genmab employees, headhunting candidates, asking for CVs and other personal information. The scam can include asking for payment for interviews or interview preparation. This communication is not coming from Genmab, we encourage people to stay alert and not to respond to these queries.</i></p>
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Dec 24th, 2022 11:17PM
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Dec 24th, 2022 11:17PM
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Genmab A/S
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Health Care
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Pharmaceuticals & Biotechnology
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cph:gen
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genmab.wd3.myworkdayjobs.com
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genmab.wd3.myworkdayjobs.com
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Dec 25th, 2022 12:00AM
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Analytical CMC Specialist
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Open
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DK001 Genmab A/S
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Copenhagen - Kalvebod Brygge 43
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DNK
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Nov 25th, 2022 12:00AM
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<p>Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. </p><p></p><p><b>The Role </b><br /> </p><p>The CMC area of Genmab is growing and looking for an Analytical CMC Subject Matter Expert (SME) to join the CMC Late Stage Manufacturing Development (LSMD) Team.</p><p></p><p>As the Analytical Subject Matter Expert (SME), you will be part of a highly dedicated and specialized CMC team leading the late stage development activities of Genmab’s proprietary antibody pipeline programs towards marketing approval (BLA/MAA).</p><p></p><p>The Analytical SME will work across project teams to support the CMC Project Managers and work closely with other SMEs for e.g. upstream processing, downstream processing, and characterization as well as with relevant SMEs within partner programs.</p><p></p><p><b>Responsibilities</b></p><p><br />The Analytical SME will be responsible for the following:</p><ul><li><p>Responsible for the LSMD analytical strategy on ongoing projects</p></li><li><p>Responsible for the day to day oversight of analytical activities performed at partnered CMOs according to latest industry standards and regulatory guidance</p></li><li><p>Prepare/review technical documents including development/validation/transfer protocols and reports</p></li><li><p>Authoring and review of CMC regulatory analytical submissions documents</p></li><li><p>Work closely with characterization SME’s to develop late stage development analytical/characterization strategies</p></li><li><p>-Support defining/refining required processes for analytical/characterization activities</p></li></ul><p></p><p><b>Requirements</b></p><ul><li><p>It is expected that you have a master’s degree in natural science, pharmacy, or similar</p></li><li><p>You have at least 5 years of documented professional experience with analytical methods for GMP manufacturing preferable from late stage development</p></li><li><p>You have a thorough understanding of the detailed requirements for analytical validation and are up to date with current trends</p></li><li><p>You preferable have active and recent experience within analytical development and validation of methods for biologics/monoclonal antibodies from a phase II/III program</p></li><li><p>You preferably have experience with chromatographic and pharmacopeia methods for biologics. Experience with other analytical methods is also desirable</p></li><li><p>You preferably have experience in establishing commercial specifications</p></li><li><p>Expertise in applied statistics for (bio)pharmaceutical manufacturing is a plus</p></li><li><p>It is preferred that you have experience in preparing and reviewing relevant filing documentation for regulatory market authorizations (e.g. BLA, MAA, J-NDA)</p></li><li><p>Excellent communication skills in English written and oral</p></li></ul><p></p><p>Moreover, you meet the following professional requirements:</p><ul><li><p>You are focused on achieving goals that are important for the team and our organization</p></li><li><p>You have the ability to work successfully under pressure in a fast-paced environment and with tight timeline</p></li><li><p>You are pro-active, take initiative and responsibility</p></li><li><p>You are a team player with demonstrated ability to collaborate with a diverse group of internal and external stakeholders</p></li><li><p>With your positive attitude you enjoy working in multicultural teams inside and outside of Genmab</p></li></ul><p></p><p><span>Genmab will offer the successful application a challenging position, where the right candidate will have the opportunity to work with highly specialised people across functions in an informal, multicultural environment, with an aim to make a difference in the lives of people with cancer.<br /><br />At Genmab, we pride ourselves on our unique culture. We are committed to make a positive impact on the lives of cancer patients. We hypothesize and experiment to seek innovative solutions, no matter the employee’s role; we speak up, empower each other, and embrace change and growth; we respect and celebrate our differences while working as one team. Teamwork and respect are central pillars of Genmab’s culture and we therefore ensure an inclusive, open, and supportive professional work environment across our international locations. Genmab employees work with determination, challenge the status quo and cultivate a growth mindset in everything we do.</span></p><p></p><p><span>We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. </span>No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability or genetic information.</p><p></p><p><span>Genmab A/S is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website: <a href="http://www.genmab.com/privacy/applicants-hr-genmab-a-s/" target="_blank">http://www.genmab.com/privacy/applicants-hr-genmab-a-s/</a></span></p><p></p><p><b><span>Scam alert</span></b></p><p><i>Please be alerted that at the moment a recruitment scam involving Genmab is circulating. The scam involves recruiters on LinkedIn and elsewhere, pretending to be Genmab employees, headhunting candidates, asking for CVs and other personal information. The scam can include asking for payment for interviews or interview preparation. This communication is not coming from Genmab, we encourage people to stay alert and not to respond to these queries.</i></p>
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Dec 24th, 2022 11:17PM
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Dec 24th, 2022 11:17PM
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Genmab A/S
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Health Care
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Pharmaceuticals & Biotechnology
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cph:gen
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genmab.wd3.myworkdayjobs.com
|
genmab.wd3.myworkdayjobs.com
|
Dec 25th, 2022 12:00AM
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Senior Clinical Trial Manager
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Open
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DK001 Genmab A/S
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Copenhagen - Kalvebod Brygge 43
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DNK
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Nov 25th, 2022 12:00AM
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<p>Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. </p><p></p><p><b>The Role</b></p><p></p><p>Are you looking for an opportunity where you can take the lead in delivering key trial management elements on oncology trials and ensure sponsor engagement?</p><p></p><p>We are looking for a (Senior) Clinical Trial Manager, someone driven by ensuring a one-team culture with CROs, and who excels in contributing to great teamwork and working environment. Join our innovative, hardworking, and ambitious team collaborating in a high-performing and fast-paced environment dedicated to improving the lives of cancer patients.</p><p></p><p>As (Senior) Clinical Trial Manager (CTM) in Clinical Operations at Genmab, you will:</p><ul><li>Lead one or more trials ensuring that key project deliverables are met with the overall goal of developing new and innovative treatments for cancer.</li><li>Lead the cross-functional trial-specific trial team, including the CROs, to deliver clinical trials within budget and timelines and according to quality standards defined by regulations, Genmab SOPs and ICH-GCP.</li></ul><p></p><p>In the Trial Management team in Clinical Operations, we are currently more than 60 highly motivated and experienced people located in Denmark, the US, the Netherlands, and Japan.</p><p></p><p>Working in Clinical Operations is exciting, intense, challenging, and fun at the same time. The dedication, collaborative and knock-your-socks-off spirit of our employees are what really shapes our team. From Day One, the onboarding program makes sure that you accomplish trainings, get settled with our IT systems and that you team up with your mentor, colleagues, and relevant stakeholders.</p><p></p><p><b>Responsibilities</b></p><p></p><p>The (Senior) Clinical Trial Manager will plan, set up and execute clinical trials and will be responsible for successful delivery of key trial management elements. The principal responsibilities are:</p><p></p><ul><li>Lead the trial team and act as the overall responsible for trial related activities from start up to reporting of a clinical trial in close collaboration with internal stakeholders and CROs</li><li>Secure trial deliverables in a proactive and motivational manner</li><li>Communicate with and perform stakeholder management of CROs and other stakeholders throughout all stages of trial conduct</li><li>Create good working environment by being a role model in great teamwork</li><li>Ensure proper documentation, record management, risk assessment/management, trial budgets, as well as sponsor engagement and sponsor oversight activities</li><li>Constantly develop and implement new and better clinical trial practices</li><li>Act as Clinical Operations representative in Compound Development Teams</li></ul><p></p><p><b>Requirements</b></p><p></p><ul><li>A BSc or MSc degree within the medical, biological, pharmaceutical science or equivalent.</li><li>Minimum of 3-4 years (7 years for Senior CTM) of experience with clinical trial management from a pharmaceutical company and/or CRO.</li><li>Experience within the field of oncology and/or first-in-human trials is preferred.</li><li>Proven skills from working in a project oriented and international organization.</li><li>Minimum 2 years’ experience as Clinical Operations representative in Clinical Development Teams (CDTs) or Global Project Teams (GPTs) would be preferable.</li><li>Excellent communication skills in English both written and spoken.</li></ul><p></p><p>Moreover, you meet the following personal requirements:</p><ul><li>Dedicated team player who enjoys leading teams and inspire trust among colleagues.</li><li>Quality mindset and able to prioritize your work in a fast paced and changing environment.</li><li>Result- and goal-oriented and committed to contributing to the overall success of Genmab.</li></ul><p></p><p></p><p><span>Genmab will offer the successful application a challenging position, where the right candidate will have the opportunity to work with highly specialised people across functions in an informal, multicultural environment, with an aim to make a difference in the lives of people with cancer.<br /><br />At Genmab, we pride ourselves on our unique culture. We are committed to make a positive impact on the lives of cancer patients. We hypothesize and experiment to seek innovative solutions, no matter the employee’s role; we speak up, empower each other, and embrace change and growth; we respect and celebrate our differences while working as one team. Teamwork and respect are central pillars of Genmab’s culture and we therefore ensure an inclusive, open, and supportive professional work environment across our international locations. Genmab employees work with determination, challenge the status quo and cultivate a growth mindset in everything we do.</span></p><p></p><p><span>We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. </span>No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability or genetic information.</p><p></p><p><span>Please note that if you are applying for a position in the Netherlands; Genmab’s policy for all permanently budgeted hires in this location is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract. </span></p><p></p><p><span>Genmab A/S is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with you application on our website <a href="https://www.genmab.com/privacy" target="_blank">https://www.genmab.com/privacy</a>. </span></p><p></p><p><b><span>Scam alert</span></b></p><p><i>Please be alerted that at the moment a recruitment scam involving Genmab is circulating. The scam involves recruiters on LinkedIn and elsewhere, pretending to be Genmab employees, headhunting candidates, asking for CVs and other personal information. The scam can include asking for payment for interviews or interview preparation. This communication is not coming from Genmab, we encourage people to stay alert and not to respond to these queries.</i></p>
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Dec 24th, 2022 11:17PM
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Dec 24th, 2022 11:17PM
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Genmab A/S
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Health Care
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Pharmaceuticals & Biotechnology
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cph:gen
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genmab.wd3.myworkdayjobs.com
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genmab.wd3.myworkdayjobs.com
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Dec 25th, 2022 12:00AM
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Associate Director, Clinical Project Lead
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Open
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DK001 Genmab A/S
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Copenhagen - Kalvebod Brygge 43
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DNK
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Nov 25th, 2022 12:00AM
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<p>Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. </p><p></p><p><b>The Role</b></p><p></p><p>Are you looking for an opportunity, where you can take the lead in the operational strategy and oversight of oncology clinical trials and ensure appropriate communication to relevant stakeholders? We are looking for a Clinical Project Lead (CPL) driven by ensuring a one-team culture and who excels in contributing to great teamwork and working environment. Join our innovative, hardworking, and ambitious team collaborating in a high performing and high pace environment to improve the lives of cancer patients.</p><p></p><p>The Clinical Project Lead is responsible for the operational strategy and oversight of one or more trials within one or more development projects. The Clinical Project Lead will join Clinical Operations with team members in Denmark, US, the Netherlands, and Japan. The Clinical Project Lead represents Clinical Operations in one or more cross-functional Compound Development Teams (CDT) and will represent one or more functional areas within the department.</p><p></p><p><b>Responsibilities</b></p><p></p><p>As Clinical Project Lead, you will:</p><ul><li><p>Provide input to the Clinical and Compound Development Plans developed by the CDT</p></li><li><p>Support the synopsis development, protocol development, document generation for Health Authorities (HA) and respond to questions from HA (as applicable), attend Key Opinion Leader (KOL)/partner meetings, give input to the overall project objectives</p></li><li><p>Ensure close and transparent communication between the CDT and the Clinical Management Team (CMT)</p></li><li><p>Support the Clinical Trial Managers (CTMs) in ensuring that the overall deliverables of the trials support the overall development strategy and timelines and within agreed budget and quality standards defined by regulations, Genmab SOPs and ICH-GCP</p></li><li><p>Take the lead in oversight of trial budget across trials and work with the CMT to ensure timely deliverables of trials in accordance with the company objectives</p></li><li><p>Drive lessons learned across trials/projects and vendors, review major findings, and ensure proper follow up</p></li><li><p>Support vendor selection, work order review and budget development at trial level</p></li><li><p>Ensure high-level communication on progress of trial deliverables and timelines to relevant stakeholders in the CDT as well as external partners as applicable and responsible for ensuring</p></li></ul><p></p><p>The employee will also give input to the department related activities, the overall department strategy and lead/support various initiatives/activities internally within the department or across departments.</p><p></p><p>The CPL may also:</p><ul><li><p>Act as CTM, if no other CTM or a less experienced CTM is assigned to a trial As CTM, the CPL will be responsible for planning, set-up and conduct of clinical trials in accordance with Genmab SOPs</p></li><li><p>Represent Clinical Operations in Project Boards, Global Development Team and Operational Committee’s/Steering Committee’s with the partners</p></li><li><p>Act as deputy for the HoD, Clinical Operations in the Protocol Review Committee, Safety Committees, and Steering Committees with the vendors</p></li></ul><p></p><p>Working in Clinical Operations is exciting, intense, challenging, and fun at the same time. The dedication, collaborative and knock-your-socks-off spirit of our employees are what really shapes our team. From day one, the onboarding program makes sure that you accomplish relevant trainings, get settled with our IT systems and that you team up with your mentor, colleagues, and relevant stakeholders.</p><h2></h2><h2><b><span>Requirements</span></b></h2><ul><li><p>A BSc or MSc level within the medical, biological, pharmaceutical science or equivalent</p></li><li><p>Minimum 7 years’ experience with clinical trial management from a pharmaceutical company and/or CRO</p></li><li><p>Experience within the field of oncology and/or first in human trials is preferred</p></li><li><p>Proven skills from working in a project oriented and international organization</p></li><li><p>Minimum 2 years’ experience as Clinical Operations representative in Clinical Development Teams (CDTs) or Global Project Teams (GPTs) would be preferable</p></li><li><p>Experience in the role as an informal leader</p></li><li><p>Excellent communication skills in English both written and spoken</p></li></ul><p></p><p>Moreover, you meet the following personal requirements:</p><ul><li><p>Dedicated team player who enjoys leading teams and inspire trust among colleagues</p></li><li><p>Quality mindset and able to prioritize your work in a fast paced and changing environment</p></li><li><p>Result- and goal-oriented and committed to contributing to the overall success of Genmab</p></li></ul><p></p><p><span>Genmab will offer the successful application a challenging position, where the right candidate will have the opportunity to work with highly specialised people across functions in an informal, multicultural environment, with an aim to make a difference in the lives of people with cancer.<br /><br />At Genmab, we pride ourselves on our unique culture. We are committed to make a positive impact on the lives of cancer patients. We hypothesize and experiment to seek innovative solutions, no matter the employee’s role; we speak up, empower each other, and embrace change and growth; we respect and celebrate our differences while working as one team. Teamwork and respect are central pillars of Genmab’s culture and we therefore ensure an inclusive, open, and supportive professional work environment across our international locations. Genmab employees work with determination, challenge the status quo and cultivate a growth mindset in everything we do.</span></p><p></p><p><span>We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. </span>No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability or genetic information.</p><p></p><p><span>Please note that if you are applying for a position in the Netherlands; Genmab’s policy for all permanently budgeted hires in this location is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract. </span></p><p></p><p><span>Genmab A/S is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with you application on our website <a href="https://www.genmab.com/privacy" target="_blank">https://www.genmab.com/privacy</a>. </span></p><p></p><p><b><span>Scam alert</span></b></p><p><i>Please be alerted that at the moment a recruitment scam involving Genmab is circulating. The scam involves recruiters on LinkedIn and elsewhere, pretending to be Genmab employees, headhunting candidates, asking for CVs and other personal information. The scam can include asking for payment for interviews or interview preparation. This communication is not coming from Genmab, we encourage people to stay alert and not to respond to these queries.</i></p>
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Dec 24th, 2022 11:17PM
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Dec 24th, 2022 11:17PM
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Genmab A/S
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Health Care
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Pharmaceuticals & Biotechnology
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cph:gen
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genmab.wd3.myworkdayjobs.com
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genmab.wd3.myworkdayjobs.com
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Dec 25th, 2022 12:00AM
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Associate Director, Global Drug Safety and Pharmacovigilance Scientist
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Open
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DK001 Genmab A/S
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Copenhagen - Kalvebod Brygge 43
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DNK
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Nov 25th, 2022 12:00AM
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<p>Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. </p><p></p><p><b>The Role</b></p><p></p><p>As Associate Director, you will become part of the Global Drug Safety and Pharmacovigilance department, where you will be responsible for drug related activities in close cooperation with the Safety Physicians. This position has a global perspective, and you will interact with stakeholders ranging from regulatory authorities and DMCs as well as colleagues from other Genmab sites.<br /> </p><p>As Associate Director, Global Drug Safety and Pharmacovigilance Scientist, you will be part of a highly skilled and international team. The position reports to the Project Safety Physician Lead.</p><p></p><p><b><span>Responsibilities</span></b></p><ul><li><p>Perform safety review of Adverse Event reports for Genmab products</p></li><li><p>Perform ongoing surveillance (including signal <span>detection/evaluation)</span> of safety data from Genmab clinical trials</p></li><li><p>Be the safety contact for other departments and ensure appropriate and timely handling of safety issues</p></li><li><p>Provide safety review and input to various documents including but not limited to: Trial Protocols, eCRFs/CRFs, and TMFs</p></li><li><p>You will also be contributing to the development of other documentation such as: Investigator’s Brochures, Subject Informed Consent, and Development Safety Update Reports</p></li><li><p>Establish and manage external Data monitoring Committees (DMCs) for early phase trials</p></li><li><p>Contribute to the planning and conduct of Safety Committee activities</p></li><li><p>Conduct safety training of Genmab employees, CROs, Investigators and other relevant site personnel as necessary</p></li><li><p>Contribute to multidisciplinary project groups including membership of the Clinical Management Team (CMT) for assigned products</p></li><li><p>Contribute to the development and optimization of new tools and process</p></li><li><p>Interact with safety and clinical CROs, perform sponsor oversight activities for safety related tasks, process invoices, and ensure regulatory compliance (including regulatory reporting requirements) for assigned products</p></li><li><p>Oversee Safety Data Exchange Agreements with partners as required</p></li><li><p>Collaborate with external experts and partners</p></li><li><p>Ensure compliance with regulatory guidelines and internal processes and procedures in order to be prepared for audits and inspections</p></li><li><p>Participate in audit and inspection activities as required</p></li></ul><p></p><p><b><span>Requirements</span></b></p><ul><li><p>University degree in life sciences (e.g. MSc Pharm., MSc Human Biology)</p></li><li><p>Solid experience (at least 5 years) within clinical trial safety</p></li><li><p>Experience within the field of oncology and monoclonal antibodies is an advantage</p></li><li><p>Good understanding of medical concepts, disease processes, scientific methodology, drug development, and data analysis</p></li><li><p>Project management skills</p></li><li><p>Strong analytical sense and curiosity</p></li><li><p>Can make independent decisions</p></li><li><p>Excellent communication skills in English both written and spoken</p></li></ul><p></p><p>Moreover, you meet the following personal requirements:</p><ul><li><p>High ethical standards, responsible, and organized with an ability to adapt and drive constant change for continuous improvement</p></li><li><p>Strong communicator, team player and good at building professional relations to collaborators and business partners</p></li><li><p>You are proactive and able to prioritize work in a fast paced and changing environment</p></li><li><p>You are result-and goal-oriented and committed to contributing to the overall success of Genmab</p></li><li><p>Thrive in a multicultural environment</p></li></ul><p></p><p><span>Genmab will offer the successful application a challenging position, where the right candidate will have the opportunity to work with highly specialised people across functions in an informal, multicultural environment, with an aim to make a difference in the lives of people with cancer.<br /><br />At Genmab, we pride ourselves on our unique culture. We are committed to make a positive impact on the lives of cancer patients. We hypothesize and experiment to seek innovative solutions, no matter the employee’s role; we speak up, empower each other, and embrace change and growth; we respect and celebrate our differences while working as one team. Teamwork and respect are central pillars of Genmab’s culture and we therefore ensure an inclusive, open, and supportive professional work environment across our international locations. Genmab employees work with determination, challenge the status quo and cultivate a growth mindset in everything we do.</span></p><p></p><p><span>We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. </span>No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability or genetic information.</p><p></p><p><span>Genmab A/S is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website: <a href="http://www.genmab.com/privacy/applicants-hr-genmab-a-s/" target="_blank">http://www.genmab.com/privacy/applicants-hr-genmab-a-s/</a></span></p><p></p><p><b><span>Scam alert</span></b></p><p><i>Please be alerted that at the moment a recruitment scam involving Genmab is circulating. The scam involves recruiters on LinkedIn and elsewhere, pretending to be Genmab employees, headhunting candidates, asking for CVs and other personal information. The scam can include asking for payment for interviews or interview preparation. This communication is not coming from Genmab, we encourage people to stay alert and not to respond to these queries.</i></p>
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Dec 24th, 2022 11:17PM
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Dec 24th, 2022 11:17PM
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Genmab A/S
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Health Care
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Pharmaceuticals & Biotechnology
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cph:gen
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genmab.wd3.myworkdayjobs.com
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genmab.wd3.myworkdayjobs.com
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Dec 25th, 2022 12:00AM
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Veeva System Manager
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Open
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DK001 Genmab A/S
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Copenhagen - Kalvebod Brygge 43
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DNK
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Nov 25th, 2022 12:00AM
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<p>Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. </p><p></p><p><b>The Role</b></p><p></p><p>Genmab is looking for a new Veeva System Manager to support the R&D organization in maintaining, developing, and supporting our global electronic document management system (EDMS) – GenDocs, covering the clinical, regulatory, CMC, and Quality Assurance areas.</p><p></p><p>Genmab´s EDMS system is a global GxP IT system based on the Veeva Vault cloud platform and it supports our dynamic and expanding R&D organization. The System Management team is a GxP IT application team, who supports and develops IT GxP systems in R&D used in the clinical, regulatory, CMC and Quality Assurance areas.</p><p></p><p>It is expected that you as our System Manager will work closely together with the line of business departments, understanding, and bridging their business needs to the system. As a System Manager, you will implement new IT functions and features in the system to improve and optimize the business processes in the line of business departments. This will be done in close collaboration with the rest of the team, the line of business departments, and the vendor of the system.</p><p></p><p>You will act as a functional lead where you participate and contribute to the configuration and development of the system with different SME´s from line of business, vendor, and our own team.</p><p></p><p>This position will be a great opportunity for you to work and develop your competences and career within global IT application management and get first-hand experience of how a biotech company operates. The position also involves communication with external vendors and with end users in line of business through projects, network groups, and daily tasks. <span>The position reports to Associate Director, R&D Business Systems Management. </span></p><p></p><p><b>Responsibilities</b></p><ul><li><p>Contribute to the optimization and innovation of the GenDocs system and their related processes in line of business</p></li><li><p>Participate in daily change- or issue-related system maintenance work in the team</p></li><li><p>Continue to improve procedures, work instructions, templates, and other tools to optimize the system and related business processes</p></li><li><p>Participate in future Veeva Vault implementation or improvement projects as Functional Lead or as Project Manager</p></li><li><p>Maintain the system compliance documentation during operation of the GenDocs system</p></li><li><p>Liaise with line of business departments and IT Business Partners to align plans and roadmaps for the future development of the system</p></li><li><p>Prepare and participate during audits and inspections of the GenDocs system</p></li></ul><p></p><p><b>Requirements</b></p><ul><li><p>We expect that you have a bachelor’s degree e.g., Life Science, IT, Engineering or similar</p></li><li><p>You have at least 5 years of experience from the pharmaceutical or biotech industry and +5 years from a similar role as System Manager</p></li><li><p>You have practical work experience with EDMS systems, and preferably Veeva Vault administrator certification</p></li><li><p>It is an advantage, but not a requirement, if you have worked in clinical development regulatory affairs or a similar area within line of business</p></li><li><p>You have extensive knowledge and understanding of GxP systems, GAMP, IT validation, and test management</p></li><li><p>You have participated in IT GxP projects, either as project SME, Functional Lead, or Project Manager</p></li><li><p>You have excellent communication skills in both Danish and English, written and oral</p></li><li><p>It is an advantage but not a requirement if you have experience with IT test tools, like HP ALM, or similar</p></li></ul><p></p><p>Moreover, you meet the following personal requirements:</p><ul><li><p>Ability to work independently as well as in teams</p></li><li><p>Service minded and a good communicator</p></li><li><p>Pragmatic attitude, able to balance, and see other´s perspective</p></li><li><p>Personal drive, and a positive attitude</p></li><li><p>Detail-oriented, structured, and takes responsibility</p></li></ul><p></p><p><span>Genmab will offer the successful application a challenging position, where the right candidate will have the opportunity to work with highly specialised people across functions in an informal, multicultural environment, with an aim to make a difference in the lives of people with cancer.<br /><br />At Genmab, we pride ourselves on our unique culture. We are committed to make a positive impact on the lives of cancer patients. We hypothesize and experiment to seek innovative solutions, no matter the employee’s role; we speak up, empower each other, and embrace change and growth; we respect and celebrate our differences while working as one team. Teamwork and respect are central pillars of Genmab’s culture and we therefore ensure an inclusive, open, and supportive professional work environment across our international locations. Genmab employees work with determination, challenge the status quo and cultivate a growth mindset in everything we do.</span></p><p></p><p><span>We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. </span>No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability or genetic information.</p><p></p><p><span>Genmab A/S is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website: <a href="http://www.genmab.com/privacy/applicants-hr-genmab-a-s/" target="_blank">http://www.genmab.com/privacy/applicants-hr-genmab-a-s/</a></span></p><p></p><p><b><span>Scam alert</span></b></p><p><i>Please be alerted that at the moment a recruitment scam involving Genmab is circulating. The scam involves recruiters on LinkedIn and elsewhere, pretending to be Genmab employees, headhunting candidates, asking for CVs and other personal information. The scam can include asking for payment for interviews or interview preparation. This communication is not coming from Genmab, we encourage people to stay alert and not to respond to these queries.</i></p>
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Dec 24th, 2022 11:17PM
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Dec 24th, 2022 11:17PM
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Genmab A/S
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Health Care
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Pharmaceuticals & Biotechnology
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cph:gen
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genmab.wd3.myworkdayjobs.com
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genmab.wd3.myworkdayjobs.com
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Dec 25th, 2022 12:00AM
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Senior Associate, Payroll Accountant
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Open
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DK001 Genmab A/S
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Copenhagen - Kalvebod Brygge 43
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DNK
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Nov 25th, 2022 12:00AM
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<p>Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. </p><p></p><p>Are you experienced with Danish payroll regulation? Are you looking for a Payroll Account position with an international aspect, working with more complex regulations? Do you want to get on-the-job training about restricted stock units and warrants? Then this could be an exciting new opportunity for you.</p><p></p><p><b><span>The Role</span></b><br /> </p><p>Based in the Copenhagen headquarters, you will be responsible for managing the payroll for Genmab’s remote workers currently located in Belgium, Austria, UK, France, Italy, and more countries to come. In addition, you will support in managing the payroll for Denmark with approx. 500 employees. The Payroll Accountant will work closely with the HR colleagues and various 3rd party payroll providers.</p><p></p><p>This is a key position within the Genmab European Accounting Operations Teams and a great opportunity for an experienced, motivated, and ambitious payroll professional. You will be working in a highly motivated team of experienced professionals in an organization where we value innovation, determination, respect, integrity, and teamwork. We are looking for candidates who will have a hands-on approach and the ability to operate a payroll function under different jurisdiction/locations.</p><p></p><p><b><span>Responsibilities</span></b></p><ul><li><p>Manage 3rd party payroll provider in locations where Genmab has employees, but no entity structure - currently Belgium, Austria, UK, France and Italy</p></li><li><p>Support in managing the payroll for the Danish legal entity with approx. 500 employees</p></li><li><p>Where integration between our HR system Workday and the payroll provider existing, it’s the responsibility of the payroll accountant to oversee and review this integration</p></li><li><p>Review payroll transactions and identify changes against master data from HR, including new hires, leave of absences, terminations, employee changes and wage garnishments, auditing payroll data and reports for errors and resolving payroll issues</p></li><li><p>Review, analyze and improve the current payroll processes to ensure a smooth run on monthly basis and compliance to SOX controls</p></li><li><p>Partner with the Payroll Manager Europe to design, document and implement procedures to streamline payroll processes</p></li><li><p>Prepare payroll journal after the payroll is processed</p></li><li><p>Prepare some payroll manual payments as and when needed</p></li><li><p>Account for RSUs & Warrants, pay the employees as needed and report accordingly to tax authorities</p></li><li><p>Prepare payroll related accruals e.g. vacation, bonuses, etc.</p></li><li><p>Accounts reconciliation for payroll related accounts</p></li><li><p>Ensure payroll compliance with company policy as well as local tax legislation</p></li><li><p>Be a business partner for the HR Operations Teams and the Global Compensation & Benefits Team to improve the overall employee experience</p></li></ul><p></p><p><b><span>Requirements</span></b></p><ul><li><p>6+ years with payroll processing in an international company</p></li><li><p>Previous experience in a regularly changing and very fast paced environment</p></li><li><p>Strong knowledge of Payroll and Benefits standard methodologies and familiarity with transactional based payroll and automated processes</p></li><li><p>Experience in equity accounting and reporting (Restricted Stock Units and Warrants) is a preference</p></li><li><p>Fluency in English</p></li><li><p>Work experience of Workday and SAP payroll and reports is a preference</p></li><li><p>Experience working with colleagues from different cultures across international offices</p></li><li><p>A critical eye and sharp analytical skills to solve the issues and challenges, especially in a regional role with many diverse country complexities and needs</p></li><li><p>Exceptional inter-personal skills, collaborative working style, and with strong verbal and written communication skills</p></li><li><p>Strong team player with ability to build and maintaining strong relationships with key internal and external stakeholders</p></li></ul><p></p><p><span>Genmab will offer the successful application a challenging position, where the right candidate will have the opportunity to work with highly specialised people across functions in an informal, multicultural environment, with an aim to make a difference in the lives of people with cancer.<br /><br />At Genmab, we pride ourselves on our unique culture. We are committed to make a positive impact on the lives of cancer patients. We hypothesize and experiment to seek innovative solutions, no matter the employee’s role; we speak up, empower each other, and embrace change and growth; we respect and celebrate our differences while working as one team. Teamwork and respect are central pillars of Genmab’s culture and we therefore ensure an inclusive, open, and supportive professional work environment across our international locations. Genmab employees work with determination, challenge the status quo and cultivate a growth mindset in everything we do.</span></p><p></p><p><span>We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. </span>No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability or genetic information.</p><p></p><p><span>Genmab A/S is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website: <a href="http://www.genmab.com/privacy/applicants-hr-genmab-a-s/" target="_blank">http://www.genmab.com/privacy/applicants-hr-genmab-a-s/</a></span></p><p></p><p><b><span>Scam alert</span></b></p><p><i>Please be alerted that at the moment a recruitment scam involving Genmab is circulating. The scam involves recruiters on LinkedIn and elsewhere, pretending to be Genmab employees, headhunting candidates, asking for CVs and other personal information. The scam can include asking for payment for interviews or interview preparation. This communication is not coming from Genmab, we encourage people to stay alert and not to respond to these queries.</i></p>
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Dec 24th, 2022 11:17PM
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Dec 24th, 2022 11:17PM
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Genmab A/S
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Health Care
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Pharmaceuticals & Biotechnology
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