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AbbVie

- NYSE:ABBV
Last Updated 2022-05-24

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Track AbbVie hiring and firing trends, filtered by title, location, type, date, category and date of posting.
Ticker Symbol Entity Name Domain As Of Date Title URL Brand Category Location Text City State Country Posted Date Number of Openings Description Salary Salary Currency Salary Description Coordinates Date Added Date Updated Sector Industry
nyse:abbv careers.abbvie.com careers.abbvie.com Nov 14th, 2021 12:00AM Senior Manager, Business Technology Solutions, Allergan Aesthetics - EEMEA Open Information Technology Dubai, Dubai, United Arab Emirates Dubai Dubai ARE Nov 4th, 2021 12:00AM About Allergan Aesthetics At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more. Our goal is to consistently provide our customers with innovation, education, exceptional service, and a commitment to excellence, all with a personal touch. For more information, visit www.AllerganAesthetics.com. In May 2020, Abbvie pharmaceuticals purchased Allergan plc, a company that contained both a pharmaceutical division and an aesthetics division with many key products including Botox and Juvederm fillers. Since the acquisition, the approach has been to combine the pharma business into the Abbvie portfolio whilst standing up a new aesthetics business, Allergan Aesthetics. With Allergan Aesthetics, the Commercial BTS function is split between US and International, the latter having responsibility of all commercial IT functions globally, outside of the US. Within the International BTS organization we are split between pure business-facing or BRM roles and other roles that are more technology-centric (“product lines”). The latter is responsible for developing class-leading capabilities whilst the former is primarily tasked with partnering with the business, understanding their objectives and working within the IT organization to bring our significant capabilities to bear in market. The role of Senior Manager, BTS EEMEA is a business relationship role and will be responsible for developing and growing the relationship within the EEMEA region. Based in Dubai, UAE the incumbent will report to the Head of BTS International, Allergan Aesthetics. We are looking for a “business leader with an IT specialism”, not a traditional technologist. To be successful in this role, you would need to be: Conversant with business strategy and metrics (P&L, SG&A, Revenue, Cost, Market Share, Market Penetration, Competitor assessment etc). People person who is able to quickly establish credibility with all levels of the organisation but mainly with senior business and IT leaders. Able to influence, negotiate and collaborate with a wide range of stakeholders to help your business get to a tangible market outcome aligned to their strategic plan. More specifically, you would: Develop and nurture a meaningful relationship with key stakeholders and own that relationship through all phases of people, process and technology changes. Able to work with business partners to understand and shape their roadmap as well as translate business roadmaps into technology roadmaps working in partnership with the Product Line organisation. Influence and own, where applicable, budget management decisions as it related to IT including advising on capital expenditure, ongoing running costs while constantly looking for opportunities to save and reinvest money. Work with the business leaders to make conscious choices of projects, i.e. sequencing, prioritisation, capacity from IT and from business to implement and adopt the change. Responsible for working with the business to assess readiness to implement solutions, ensuring seamless implementations and post go-live follow ups. Able to define, track and report on adoption and utilisation metrics and works with the business to actively increase awareness and utilisation of assets. Ensure, in conjunction with IT and business partners, a state of full compliance and audit readiness. Able to intimately understand key business processes and translate that to product owners. Work with the Product Owners to build out capabilities and service catalogue items. Will work with other IT service providers to deliver services to the business. Advocate for reduction in business and technical complexity, pull through of regional and global initiatives and actively works to reduce inhouse systems (where appropriate) Be a thought leader to help inform and shape both the business and IT strategy. Have breath in terms of understanding technology offerings and systems, not necessarily depth although that might be useful in a commercial context (Sales, Marketing, Digital). The current scope of the AA BTS technology solutions and services include: Sales and Sales Force Effectiveness Customer Relationship Management Digital Marketing, Websites/Portals E-Commerce Marketing Resource Management and Digital Asset Management Electronic promotional material, including Closed Loop Marketing Master Data Management Data Warehouse/BI Performance Management Financial Compliance Internal Collaboration External Stakeholder Solutions Qualifications Minimum Bachelors degree in information technology, digital marketing and/or Business management Minimum 15+ years of related experience and success in working in a business centric, complex, progressive, multi-stakeholder, matrix environment, with at least five in a digital product development or Business relationship management role. Innovative - keep up with latest technology and trends. Experience in digital product development or digital transformation. Proven success in implementing digital and innovative solution. Strong leadership skills with proven ability to manage change and drive innovation. Experience in leading IT and business into new technologies and open to new ideas. Strong ability to connect unrelated concepts and generate original or unique ideas Strong Business engagement, interpreting business needs into technology solutions. Communicate effectively with both technical and business leadership to ensure successful deployment for both localization of global platforms or local proprietary needs. Demonstrated ability to influence and advise executive leadership on the best use of technology; as well as justify and lead large scale commercial programs Demonstrated ability to work closely with the business, and partner with them in developing IT systems Strong ability to de-mystify complex technical subjects and ideas for non-technical audiences Strong business and financial acumen Experience in shaping IT portfolio aligning business priorities to key technology strategies. Extensive experience working with remote teams, and with vendor resources Experience in high performing matrix environment and collaboration \ Global organizations. Proven track record of leading and organizing cross-functional project teams and working across organizational boundaries Knowledge of business process mapping, and diverse systems environments; with focus in SFDC technology stacks, e-commerce technologies, and data warehousing and analytics. Expertise in agile or iterative project execution methodologies. Proven track record in transforming, building and leading effective IT organizations Proven track record of being able to work under pressure or conflict in a very methodical, responsible and constructive way and be a role model for the organization Experience in implementing IT systems and ensuring end to end IT services delivery for a large business organization or area. Preferred Qualifications: MBA or Master’s degree Business Technology consulting experience Experience in introducing/delivering technology solutions that build brand loyalty and improve/enhance customer or consumer experience. Experience in working in a regulated business Experience with CRM, SFA, electronic promotional material development (closed-loop marketing, websites, portals, iPad apps) or digital marketing Healthcare related experience is preferred but not a must. Experience in FMCG or Aesthetics is a plus Travel Yes, 10 % of the Time Job Type Experienced Schedule Full-time Job Level Code IC About AbbVie AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. POINT (55.2707828 25.2048493) Nov 13th, 2021 09:42PM Nov 13th, 2021 09:42PM Health Care Pharmaceuticals & Biotechnology
nyse:abbv careers.abbvie.com careers.abbvie.com Nov 14th, 2021 12:00AM Area Site Management Lead Open Clinical Research Argentina ARG Sep 24th, 2021 12:00AM About AbbVie AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Purpose: The Area Site Management Lead is responsible and accountable for directing CRAs in a matrix environment and for driving the successful execution of Clinical Site Management (CSM) study deliverables for their assigned studies within their geographical Area. ASMLs are study experts and provide monitoring expertise and ensure on-time and quality CSM deliverables (data, monitoring plan, SOPs, regulations). Review site and CRA outputs for compliance with protocol and monitoring plans. Function as a liaison and primary contact between CRAs and GSML. Primary responsibilities include but not limited to: Manage and oversee day-to-day monitoring activities on assigned study/is to ensure CSM deliverables are met by tracking and maintaining project metrics and status of deliverables. Proactively communicate and escalate issues, risks and mitigation plans to Area/Country Leadership and GSML. Proactively communicate and support planning with Country teams (COM / CCOM) the CSM resources in alignment with the study deliverables and milestones. Proactive support and management of database lock efforts Primary point of contact for CRAs for study and site questions. Ensure country/area planned/LBEs timelines are aligned with overall study planning. Accountable for creating and driving recruitment plans for their assigned study(is) within their geographic Area. Accountable for delivering site selection per targets at country/area level. Represent Area as part of a coordinated study leadership team directed by the GSML in the delivery of on-time and on-target quality CSM deliverables. Review completed Site Feasibility Questionnaires, ensures adherence to monitoring plans (SEV, STV, on-site/off-site, COV) for assigned study/is. Conduct trending, assessment of risk, mitigation plans, root cause analysis for issues and emerging issues. Partner with GSML and C/COM on issue identification and addressing issues. Develop monitoring tools for trial, drive implementation and ensure consistency across area. Provide monitoring plan training and ongoing non-clinical CRA training. Conduct CRA teleconferences to deliver training and information as required. Attend study team meetings as applicable and disseminate information, as necessary. Collaborate with GSML in review of study specific eCRFs, completion guidelines, protocol deviation specifications, user acceptance testing, etc. Liaise with study-start-up to ensure timely site start-up. Accountable for recruitment across assigned areas/studies and collaborate with other ASMLs/GSML to accomplish recruitment for the trial. Ensure accuracy, completeness and timeliness of TESLA and other systems (e.g., LBEs for site/country events/milestones) Ensure issues/observations are entered, escalated, and actioned in a timely manner. Analyze for emerging trends and escalate to GSML and Area leadership as appropriate. Contribute to ongoing process improvement initiatives within their geographic area. Work across areas or globally depending on site distribution. Serve as an AdaptiV ambassador ensuring implementation and ensuring risk-based thinking on trial. May conduct joint visits with CRAs at challenging sites, as needed. Ensures audit/inspection readiness at country/site level, incl. TMF completeness. Maintain knowledge of ICH/GCP, regulatory requirements, AbbVie SOPs, therapeutic area (protocol, amendments). Qualifications Qualifications: Bachelor’s Degree or equivalent OUS degree, typically in (para)medical or scientific field. A minimum of 5 – 7 years of industry clinical research experience including 2 years of monitoring or equivalent experience. Prefer candidates that have functioned as a lead CRA/ have equivalent experience. Experience in multiple therapeutic areas or disease state/indications highly desired. Strong analytical and critical thinking skills and the ability to evaluate complex issues from multiple perspectives and drive smart decision making. Excellent interpersonal skills with the ability to build trust, communicate with influence, clarity, flexibility, and adaptability to changing requirements. Excellent planning, organizing and proactive prioritization skills; ability to work effectively and efficiently in a dynamic, fast-paced environment. Ability to create and deliver presentations. Able to work well within a matrix team in a fast-paced environment managing multiple priorities. Computer Literacy: Advanced skills in Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft OneNote Travel Yes, 25 % of the Time Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. POINT (-63.616672 -38.416097) Nov 13th, 2021 09:42PM Nov 13th, 2021 09:42PM Health Care Pharmaceuticals & Biotechnology
nyse:abbv careers.abbvie.com careers.abbvie.com Nov 14th, 2021 12:00AM 1MBA Commercial Early Career Program - Argentina Open Marketing Buenos Aires, Argentina Buenos Aires ARG Jun 22nd, 2021 12:00AM About AbbVie AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. As a Latin America Commercial Early Career Program Argentina member, you’ll participate in a new, full-time rotational program supporting our Latin America affiliate. This program helps develop high potential MBA talent for future commercial and management positions. By rotating through a variety of Latin America commercial roles across AbbVie over two years and three rotations, the program addresses the business needs of today while helping to grow experienced, well-rounded management talent for tomorrow. You will also get experience by working cross functionally in a matrix environment, building your business acumen, and participating in key training sessions. Key Responsibilities Include: • Market access planning and execution • Infield Team planning and execution • Training program development • Creation of a patient support program for new products • Demonstrated oral and written communication skills • Strong analytical skills • Demonstrated leadership potential • Strong track record of accomplishments • Prior work experience in business or sales Qualifications • IMPORTANT: you must have recently finished (no longer than 2 years ago) your Master’s of Business Administration, preferably with an emphasis on marketing or general management. • Strong academic performance, minimum cumulative GPA = 3.0/4.0 • Fluency in Spanish or Portuguese (reading, writing, and speaking) • Eligible to work in Argentina . On a permanent basis without requiring sponsorship. • Geographic mobility, interested in a career in Latin America Locations Assignment opportunities are in the following cities: • .Argentina. Travel Yes, 15 % of the Time Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. POINT (-58.3815591 -34.6036844) Nov 13th, 2021 09:42PM Nov 13th, 2021 09:42PM Health Care Pharmaceuticals & Biotechnology
nyse:abbv careers.abbvie.com careers.abbvie.com Nov 14th, 2021 12:00AM Regulatory Affairs Specialist Open Regulatory Affairs Buenos Aires, Argentina Buenos Aires ARG Nov 2nd, 2021 12:00AM About AbbVie AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Key responsibilities ANMAT Related Activities: Responsible for making the dossier preparation, presentation, and the submission with the Regulatory Body, for attestations and pharmaceutical plants certifications. Support the RA Team with regulatory processes such as new registrations, renewals, variations, manufacturing sites inspections. In addition to that, in charge of coordinating appointments with the Regulatory Body for submissions or retrieval of documents. Also, in charge of managing the follow-up of filings, to make sure they do not take longer than expected and are approved in accelerated timelines. Promotional Materials: Back up for the revision of promotional and non-promotional materials in Region South. Artworks: Cooperate in the revision and development of artworks for the products commercialized in the region, assuring the quality control is in place. Importation and Testing: Co- lead the activities leading to importation, notification of analysis dates and results of local testing for imported products, leading to release to the Argentinean market. Respond to MOH requirements on these filings. Archiving: Maintenance of the updated, complete, and orderly physical/ electronic files for both Legacies. Internal Procedures: Co- lead the review and update of applicable SOPs. Also participate in the update of local changes coming from global SOPs. Customers: Back- up for the revision of regulatory documentation from customers in the opening account process and periodically afterwards. Key activity to assure the products are commercialized through the legally accepted chain. Budgent Management: Support the RA Direction in the tracking of expenses, vendor invoicing and payment, and internal purchase orders. Qualifications Qualifications Pharmacist - Biochemist or Biotechnologist 2 – 3 years experience on Regulatory Affairs Good communication skills Good organizational skills Travel No Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. POINT (-58.3815591 -34.6036844) Nov 13th, 2021 09:42PM Nov 13th, 2021 09:42PM Health Care Pharmaceuticals & Biotechnology
nyse:abbv careers.abbvie.com careers.abbvie.com Nov 14th, 2021 12:00AM MBA Commercial Early Career Program - Chile Open Sales Support Chile Chilecito La Rioja Province ARG Oct 29th, 2021 12:00AM About AbbVie AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. As a Latin America Commercial Early Career Program - Chile member, you’ll participate in a new, full-time rotational program supporting our Latin America affiliate. This program helps develop high potential MBA talent for future commercial and management positions. By rotating through a variety of Latin America commercial roles across AbbVie over two years and three rotations, the program addresses the business needs of today while helping to grow experienced, well-rounded management talent for tomorrow. You will also get experience by working cross functionally in a matrix environment, building your business acumen, and participating in key training sessions. Key Responsibilities Include: • Market access planning and execution • Infield Team planning and execution • Training program development • Creation of a patient support program for new products • Demonstrated oral and written communication skills • Strong analytical skills • Demonstrated leadership potential • Strong track record of accomplishments • Prior work experience in business or sales Qualifications Qualifications: • IMPORTANT: you must have recently finished (no longer than 2 years ago) your Master of Business Administration, preferably with an emphasis on marketing or general management. • Strong academic performance, minimum cumulative GPA = 3.0/4.0 • Fluency in Spanish or Portuguese (reading, writing, and speaking) • Eligible to work in Chile. On a permanent basis without requiring sponsorship. • Geographic mobility, interested in a career in Latin America • Chile. Travel No Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. POINT (-71.542969 -35.675147) Nov 13th, 2021 09:42PM Nov 13th, 2021 09:42PM Health Care Pharmaceuticals & Biotechnology
nyse:abbv careers.abbvie.com careers.abbvie.com Nov 14th, 2021 12:00AM Senior Clinical Research Associate Open Clinical Research Australia Sydney NSW AUS Aug 17th, 2021 12:00AM About AbbVie AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. For assigned sites/study(s), ensure successful protocol level execution of SMM deliverables involving start-up, execution, and close-out. Ensure site related study execution including but not limited to monitoring visits, site evaluations, site selection, and activation, and monitoring close out and visit reports. Anticipate and identify site issues that could affect timelines and develop alternative solutions. Ensure clinical trial management systems containing all site-specific information are maintained and kept current. Provide Local regulatory and legal requirement expertise. Ensures timely payment execution for the assigned sites/study(s) according to the clinical study agreements and as per local requirements. Ensure adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research. Stay abreast of new and/or evolving local regulations, guidelines and policies. Ensure audit and inspection readiness of assigned sites. Advise on pre-audit activities for GCP requirements. Prepare and follow up site audits/inspections; provide input into the CAPA preparation. Responsible for coaching and mentoring CRAs and providing input into their development. Responsible for mentoring CRAs for various aspects of work. May be responsible for being the country point of contact for CROs for an assigned study. May participate/lead in global/local task forces and initiatives. Responsible for activities as assigned by manager. If assigned; Responsible for identifying training needs and standardizing and facilitating training solutions for SMM monitors globally. Provide consistent best practice approach to onboarding, consolidating “lessons learned” across areas and incorporating into monitoring training materials, defining best practice training curriculum, and maintaining awareness of upcoming changes to ensure effective training is delivered in a timely manner. If assigned; With guidance, may serve as key point of contact in country/district for assigned study. Update Impact/Tesla with country-level information: Country-level planning timelines, LSR assignments, etc. If assigned; Global Representative for a single or multiple studies, collaborating with key stakeholders to achieve proactive, strategic and tactical success throughout the study planning, execution, and closeout phases leading to World Class clinical trials. If assigned; Responsible for remote data review of assigned sites/studies according to the Integrated Data Review Plan (IDRP), Monitoring Plan, SOP/WI and in accordance with the study timelines and objectives. Provides feedback on investigators/sites on an on-going basis based on the site performance. Interacts and builds professional and collaborative relationships with peers and site monitors. Qualifications Education: Bachelors or equivalent degree, health related (e.g. Medical, Scientific, Nursing, Pharmacy) preferred. Site Monitoring Experience: Minimum 3 years. Strong analytical and critical thinking skills to evaluate complex issues from multiple perspectives and drive smart decision making. Excellent interpersonal skills with the ability to communicate persuasively and with clarity, flexibility and adaptability to changing requirements, resourcefulness and creativity. Demonstrated proactive and positive team player. Exhibits strong planning and organizational skills and high level of flexibility in a dynamic environment with competing projects and deadlines. Demonstrated business ethics and integrity. Travel Yes, 75 % of the Time Job Type Temporary Work Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. POINT (133.775136 -25.274398) Nov 13th, 2021 09:42PM Nov 13th, 2021 09:42PM Health Care Pharmaceuticals & Biotechnology
nyse:abbv careers.abbvie.com careers.abbvie.com Nov 14th, 2021 12:00AM Senior Clinical Research Associate Open Clinical Research Australia Sydney NSW AUS Aug 31st, 2021 12:00AM About AbbVie AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. For assigned sites/study(s), ensure successful protocol level execution of SMM deliverables involving start-up, execution, and close-out. Ensure site related study execution including but not limited to monitoring visits, site evaluations, site selection, and activation, and monitoring close out and visit reports. Anticipate and identify site issues that could affect timelines and develop alternative solutions. Ensure clinical trial management systems containing all site-specific information are maintained and kept current. Provide Local regulatory and legal requirement expertise. Ensures timely payment execution for the assigned sites/study(s) according to the clinical study agreements and as per local requirements. Ensure adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research. Stay abreast of new and/or evolving local regulations, guidelines and policies. Ensure audit and inspection readiness of assigned sites. Advise on pre-audit activities for GCP requirements. Prepare and follow up site audits/inspections; provide input into the CAPA preparation. Responsible for coaching and mentoring CRAs and providing input into their development. Responsible for mentoring CRAs for various aspects of work. May be responsible for being the country point of contact for CROs for an assigned study. May participate/lead in global/local task forces and initiatives. Responsible for activities as assigned by manager. If assigned; Responsible for identifying training needs and standardizing and facilitating training solutions for SMM monitors globally. Provide consistent best practice approach to onboarding, consolidating “lessons learned” across areas and incorporating into monitoring training materials, defining best practice training curriculum, and maintaining awareness of upcoming changes to ensure effective training is delivered in a timely manner. If assigned; With guidance, may serve as key point of contact in country/district for assigned study. Update Impact/Tesla with country-level information: Country-level planning timelines, LSR assignments, etc. If assigned; Global Representative for a single or multiple studies, collaborating with key stakeholders to achieve proactive, strategic and tactical success throughout the study planning, execution, and closeout phases leading to World Class clinical trials. If assigned; Responsible for remote data review of assigned sites/studies according to the Integrated Data Review Plan (IDRP), Monitoring Plan, SOP/WI and in accordance with the study timelines and objectives. Provides feedback on investigators/sites on an on-going basis based on the site performance. Interacts and builds professional and collaborative relationships with peers and site monitors. Qualifications Education: Bachelors or equivalent degree, health related (e.g. Medical, Scientific, Nursing, Pharmacy) preferred. Site Monitoring Experience: Minimum 3 years. Strong analytical and critical thinking skills to evaluate complex issues from multiple perspectives and drive smart decision making. Excellent interpersonal skills with the ability to communicate persuasively and with clarity, flexibility and adaptability to changing requirements, resourcefulness and creativity. Demonstrated proactive and positive team player. Exhibits strong planning and organizational skills and high level of flexibility in a dynamic environment with competing projects and deadlines. Demonstrated business ethics and integrity. Travel Yes, 50 % of the Time Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. POINT (133.775136 -25.274398) Nov 13th, 2021 09:42PM Nov 13th, 2021 09:42PM Health Care Pharmaceuticals & Biotechnology
nyse:abbv careers.abbvie.com careers.abbvie.com Nov 14th, 2021 12:00AM Senior Clinical Research Associate Open Clinical Research Australia Sydney NSW AUS Sep 28th, 2021 12:00AM About AbbVie AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. For assigned sites/study(s), ensure successful protocol level execution of SMM deliverables involving start-up, execution, and close-out. Ensure site related study execution including but not limited to monitoring visits, site evaluations, site selection, and activation, and monitoring close out and visit reports. Anticipate and identify site issues that could affect timelines and develop alternative solutions. Ensure clinical trial management systems containing all site-specific information are maintained and kept current. Provide Local regulatory and legal requirement expertise. Ensures timely payment execution for the assigned sites/study(s) according to the clinical study agreements and as per local requirements. Ensure adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research. Stay abreast of new and/or evolving local regulations, guidelines and policies. Ensure audit and inspection readiness of assigned sites. Advise on pre-audit activities for GCP requirements. Prepare and follow up site audits/inspections; provide input into the CAPA preparation. Responsible for coaching and mentoring CRAs and providing input into their development. Responsible for mentoring CRAs for various aspects of work. May be responsible for being the country point of contact for CROs for an assigned study. May participate/lead in global/local task forces and initiatives. Responsible for activities as assigned by manager. If assigned; Responsible for identifying training needs and standardizing and facilitating training solutions for SMM monitors globally. Provide consistent best practice approach to onboarding, consolidating “lessons learned” across areas and incorporating into monitoring training materials, defining best practice training curriculum, and maintaining awareness of upcoming changes to ensure effective training is delivered in a timely manner. If assigned; With guidance, may serve as key point of contact in country/district for assigned study. Update Impact/Tesla with country-level information: Country-level planning timelines, LSR assignments, etc. If assigned; Global Representative for a single or multiple studies, collaborating with key stakeholders to achieve proactive, strategic and tactical success throughout the study planning, execution, and closeout phases leading to World Class clinical trials. If assigned; Responsible for remote data review of assigned sites/studies according to the Integrated Data Review Plan (IDRP), Monitoring Plan, SOP/WI and in accordance with the study timelines and objectives. Provides feedback on investigators/sites on an on-going basis based on the site performance. Interacts and builds professional and collaborative relationships with peers and site monitors. Qualifications Education: Bachelors or equivalent degree, health related (e.g. Medical, Scientific, Nursing, Pharmacy) preferred. Site Monitoring Experience: Minimum 3 years. Strong analytical and critical thinking skills to evaluate complex issues from multiple perspectives and drive smart decision making. Excellent interpersonal skills with the ability to communicate persuasively and with clarity, flexibility and adaptability to changing requirements, resourcefulness and creativity. Demonstrated proactive and positive team player. Exhibits strong planning and organizational skills and high level of flexibility in a dynamic environment with competing projects and deadlines. Demonstrated business ethics and integrity. Travel Yes, 25 % of the Time Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. POINT (133.775136 -25.274398) Nov 13th, 2021 09:42PM Nov 13th, 2021 09:42PM Health Care Pharmaceuticals & Biotechnology
nyse:abbv careers.abbvie.com careers.abbvie.com Nov 13th, 2021 12:00AM Senior Manager, Business Technology Solutions, Allergan Aesthetics - EEMEA Open Information Technology Dubai, Dubai, United Arab Emirates Dubai Dubai ARE Nov 4th, 2021 12:00AM About Allergan Aesthetics At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more. Our goal is to consistently provide our customers with innovation, education, exceptional service, and a commitment to excellence, all with a personal touch. For more information, visit www.AllerganAesthetics.com. In May 2020, Abbvie pharmaceuticals purchased Allergan plc, a company that contained both a pharmaceutical division and an aesthetics division with many key products including Botox and Juvederm fillers. Since the acquisition, the approach has been to combine the pharma business into the Abbvie portfolio whilst standing up a new aesthetics business, Allergan Aesthetics. With Allergan Aesthetics, the Commercial BTS function is split between US and International, the latter having responsibility of all commercial IT functions globally, outside of the US. Within the International BTS organization we are split between pure business-facing or BRM roles and other roles that are more technology-centric (“product lines”). The latter is responsible for developing class-leading capabilities whilst the former is primarily tasked with partnering with the business, understanding their objectives and working within the IT organization to bring our significant capabilities to bear in market. The role of Senior Manager, BTS EEMEA is a business relationship role and will be responsible for developing and growing the relationship within the EEMEA region. Based in Dubai, UAE the incumbent will report to the Head of BTS International, Allergan Aesthetics. We are looking for a “business leader with an IT specialism”, not a traditional technologist. To be successful in this role, you would need to be: Conversant with business strategy and metrics (P&L, SG&A, Revenue, Cost, Market Share, Market Penetration, Competitor assessment etc). People person who is able to quickly establish credibility with all levels of the organisation but mainly with senior business and IT leaders. Able to influence, negotiate and collaborate with a wide range of stakeholders to help your business get to a tangible market outcome aligned to their strategic plan. More specifically, you would: Develop and nurture a meaningful relationship with key stakeholders and own that relationship through all phases of people, process and technology changes. Able to work with business partners to understand and shape their roadmap as well as translate business roadmaps into technology roadmaps working in partnership with the Product Line organisation. Influence and own, where applicable, budget management decisions as it related to IT including advising on capital expenditure, ongoing running costs while constantly looking for opportunities to save and reinvest money. Work with the business leaders to make conscious choices of projects, i.e. sequencing, prioritisation, capacity from IT and from business to implement and adopt the change. Responsible for working with the business to assess readiness to implement solutions, ensuring seamless implementations and post go-live follow ups. Able to define, track and report on adoption and utilisation metrics and works with the business to actively increase awareness and utilisation of assets. Ensure, in conjunction with IT and business partners, a state of full compliance and audit readiness. Able to intimately understand key business processes and translate that to product owners. Work with the Product Owners to build out capabilities and service catalogue items. Will work with other IT service providers to deliver services to the business. Advocate for reduction in business and technical complexity, pull through of regional and global initiatives and actively works to reduce inhouse systems (where appropriate) Be a thought leader to help inform and shape both the business and IT strategy. Have breath in terms of understanding technology offerings and systems, not necessarily depth although that might be useful in a commercial context (Sales, Marketing, Digital). The current scope of the AA BTS technology solutions and services include: Sales and Sales Force Effectiveness Customer Relationship Management Digital Marketing, Websites/Portals E-Commerce Marketing Resource Management and Digital Asset Management Electronic promotional material, including Closed Loop Marketing Master Data Management Data Warehouse/BI Performance Management Financial Compliance Internal Collaboration External Stakeholder Solutions Qualifications Minimum Bachelors degree in information technology, digital marketing and/or Business management Minimum 15+ years of related experience and success in working in a business centric, complex, progressive, multi-stakeholder, matrix environment, with at least five in a digital product development or Business relationship management role. Innovative - keep up with latest technology and trends. Experience in digital product development or digital transformation. Proven success in implementing digital and innovative solution. Strong leadership skills with proven ability to manage change and drive innovation. Experience in leading IT and business into new technologies and open to new ideas. Strong ability to connect unrelated concepts and generate original or unique ideas Strong Business engagement, interpreting business needs into technology solutions. Communicate effectively with both technical and business leadership to ensure successful deployment for both localization of global platforms or local proprietary needs. Demonstrated ability to influence and advise executive leadership on the best use of technology; as well as justify and lead large scale commercial programs Demonstrated ability to work closely with the business, and partner with them in developing IT systems Strong ability to de-mystify complex technical subjects and ideas for non-technical audiences Strong business and financial acumen Experience in shaping IT portfolio aligning business priorities to key technology strategies. Extensive experience working with remote teams, and with vendor resources Experience in high performing matrix environment and collaboration \ Global organizations. Proven track record of leading and organizing cross-functional project teams and working across organizational boundaries Knowledge of business process mapping, and diverse systems environments; with focus in SFDC technology stacks, e-commerce technologies, and data warehousing and analytics. Expertise in agile or iterative project execution methodologies. Proven track record in transforming, building and leading effective IT organizations Proven track record of being able to work under pressure or conflict in a very methodical, responsible and constructive way and be a role model for the organization Experience in implementing IT systems and ensuring end to end IT services delivery for a large business organization or area. Preferred Qualifications: MBA or Master’s degree Business Technology consulting experience Experience in introducing/delivering technology solutions that build brand loyalty and improve/enhance customer or consumer experience. Experience in working in a regulated business Experience with CRM, SFA, electronic promotional material development (closed-loop marketing, websites, portals, iPad apps) or digital marketing Healthcare related experience is preferred but not a must. Experience in FMCG or Aesthetics is a plus Travel Yes, 10 % of the Time Job Type Experienced Schedule Full-time Job Level Code IC About AbbVie AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. POINT (55.2707828 25.2048493) Nov 12th, 2021 09:42PM Nov 12th, 2021 09:42PM Health Care Pharmaceuticals & Biotechnology
nyse:abbv careers.abbvie.com careers.abbvie.com Nov 13th, 2021 12:00AM Area Site Management Lead Open Clinical Research Argentina ARG Sep 24th, 2021 12:00AM About AbbVie AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Purpose: The Area Site Management Lead is responsible and accountable for directing CRAs in a matrix environment and for driving the successful execution of Clinical Site Management (CSM) study deliverables for their assigned studies within their geographical Area. ASMLs are study experts and provide monitoring expertise and ensure on-time and quality CSM deliverables (data, monitoring plan, SOPs, regulations). Review site and CRA outputs for compliance with protocol and monitoring plans. Function as a liaison and primary contact between CRAs and GSML. Primary responsibilities include but not limited to: Manage and oversee day-to-day monitoring activities on assigned study/is to ensure CSM deliverables are met by tracking and maintaining project metrics and status of deliverables. Proactively communicate and escalate issues, risks and mitigation plans to Area/Country Leadership and GSML. Proactively communicate and support planning with Country teams (COM / CCOM) the CSM resources in alignment with the study deliverables and milestones. Proactive support and management of database lock efforts Primary point of contact for CRAs for study and site questions. Ensure country/area planned/LBEs timelines are aligned with overall study planning. Accountable for creating and driving recruitment plans for their assigned study(is) within their geographic Area. Accountable for delivering site selection per targets at country/area level. Represent Area as part of a coordinated study leadership team directed by the GSML in the delivery of on-time and on-target quality CSM deliverables. Review completed Site Feasibility Questionnaires, ensures adherence to monitoring plans (SEV, STV, on-site/off-site, COV) for assigned study/is. Conduct trending, assessment of risk, mitigation plans, root cause analysis for issues and emerging issues. Partner with GSML and C/COM on issue identification and addressing issues. Develop monitoring tools for trial, drive implementation and ensure consistency across area. Provide monitoring plan training and ongoing non-clinical CRA training. Conduct CRA teleconferences to deliver training and information as required. Attend study team meetings as applicable and disseminate information, as necessary. Collaborate with GSML in review of study specific eCRFs, completion guidelines, protocol deviation specifications, user acceptance testing, etc. Liaise with study-start-up to ensure timely site start-up. Accountable for recruitment across assigned areas/studies and collaborate with other ASMLs/GSML to accomplish recruitment for the trial. Ensure accuracy, completeness and timeliness of TESLA and other systems (e.g., LBEs for site/country events/milestones) Ensure issues/observations are entered, escalated, and actioned in a timely manner. Analyze for emerging trends and escalate to GSML and Area leadership as appropriate. Contribute to ongoing process improvement initiatives within their geographic area. Work across areas or globally depending on site distribution. Serve as an AdaptiV ambassador ensuring implementation and ensuring risk-based thinking on trial. May conduct joint visits with CRAs at challenging sites, as needed. Ensures audit/inspection readiness at country/site level, incl. TMF completeness. Maintain knowledge of ICH/GCP, regulatory requirements, AbbVie SOPs, therapeutic area (protocol, amendments). Qualifications Qualifications: Bachelor’s Degree or equivalent OUS degree, typically in (para)medical or scientific field. A minimum of 5 – 7 years of industry clinical research experience including 2 years of monitoring or equivalent experience. Prefer candidates that have functioned as a lead CRA/ have equivalent experience. Experience in multiple therapeutic areas or disease state/indications highly desired. Strong analytical and critical thinking skills and the ability to evaluate complex issues from multiple perspectives and drive smart decision making. Excellent interpersonal skills with the ability to build trust, communicate with influence, clarity, flexibility, and adaptability to changing requirements. Excellent planning, organizing and proactive prioritization skills; ability to work effectively and efficiently in a dynamic, fast-paced environment. Ability to create and deliver presentations. Able to work well within a matrix team in a fast-paced environment managing multiple priorities. Computer Literacy: Advanced skills in Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft OneNote Travel Yes, 25 % of the Time Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. POINT (-63.616672 -38.416097) Nov 12th, 2021 09:42PM Nov 12th, 2021 09:42PM Health Care Pharmaceuticals & Biotechnology

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