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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 Company Name Sector Industry
nasdaq:arwr arrowheadpharmaceuticals.applytojob.com arrowheadpharmaceuticals.applytojob.com Dec 7th, 2021 12:00AM Sr. Clinical Research Associate Open Clinical Operations Pasadena CA USA The Position The Sr. Clinical Research Associate (Sr. CRA) provides support to the Clinical Operations Manager (COM)/Study Lead(s) to manage and track key study deliverables. The primary purpose of the position is to support the COM/Study Lead in study set-up, execution, and closeout to ensure study deliverables are met and compliance with clinical protocols, their objectives and ICH and GCP guidelines. This is primarily an in-house role. Responsibilities Support Study Lead to execute study milestones against study timelines   Tracking of key deliverables during start-up, study maintenance and close-out; generate, review and distribute reports from internal tracking at requested intervals (Site Status, Enrollment, Dosing) Collaborate with the Study Lead to develop/review certain study-specific plans and/or processes  Present updates at team meetings as needed (i.e., Clinical Trial Team Meeting, Project Team Meeting, Investigator Meeting, project training, etc.)  Collect and review essential documents from investigational sites Support CTAs with TMF set-up, maintenance, ongoing quality review, and final reconciliation of study documents Participate in study specific tasks such as investigator identification and site activation  Contribute to the development/review of study specific Monitoring Plans; track timing/planning of site visits to ensure compliance Contribute to the development/review of study materials, case report forms (CRFs), informed consent documents for clinical studies Review monitoring visit reports and perform occasional co-monitoring visits with CRO CRAs  Assist in the preparation and review of site reference materials (i.e., screening/enrollment logs, Delegation of Site Responsibilities form, Site Monitoring Log, etc.)  Act as CROs’ CRA/CTA first line of contact for study related questions/issues   Work with the CRO to arrange and prepare for Site Qualification Visits, Site Initiation Visits and Site Investigator Meetings (as applicable)  Provide updates on study/site status as needed to ensure timely study entry and updates are reflected on ClinicalTrials.gov or EU equivalent Assist Study Lead with design and preparation of study related materials for the training of CRO staff  Assist Study Lead with oversight of study vendors (CRO, Drug Supply, Central Lab) as required  Perform remote query and data review as needed to assist CDM  Assist clinical finance and study lead with the review, tracking and management of study specific budgets Required:  4-year college degree (preferred) otherwise, candidates with a combination of education and relevant experience will be considered Minimum of five (5) years in clinical research Minimum of three (3) years onsite monitoring/site management experience Experience managing/supervising vendors Thorough understanding of all applicable FDA ICH- GCP regulations and guidelines Working knowledge of medical terminology Ability to proactively perform and complete duties with minimal supervision in an accurate and timely manner Proficient in MS Office (Word, Excel, and PowerPoint) Ability to work in a team or independently  Effective interpersonal, written and verbal communication skills  Able to critically evaluate job tasks and the impact on overall study execution  Strong problem-solving capabilities  Effectively collaborates with Study Team members  Exceptional organizational skills with the ability to multi-task and prioritize  Attention to detail Ability to work with distributed team members and outside vendors Occasional travel in US or overseas (<10%) Preferred:  CRA certification Dec 6th, 2021 09:20PM Dec 6th, 2021 09:20PM Arrowhead Research Health Care Pharmaceuticals & Biotechnology
nasdaq:arwr arrowheadpharmaceuticals.applytojob.com arrowheadpharmaceuticals.applytojob.com Dec 7th, 2021 12:00AM Director, Organization Learning & Development Open Human Resources Pasadena CA USA The PositionArrowhead is seeking an experienced, hands-on Director, Organizational Learning & Development to design and deliver effective Company-wide leadership and team development programs to enhance team and individual competencies, development and performance. The Director, OLD will partner with senior management and function leaders to identify needs and opportunities to further the successful growth of the company by applying thoughtful, intentional initiatives directed to achieving Arrowhead’s strategic and operational goals.ResponsibilitiesConsult with senior management and function leaders on needs pertaining to the development of the organization, offer expert advice and guidance to assist with organizational learning and development related topicsPartner with HR team and other key stakeholders in the organization to develop and promote consistent cultural and behavioral messages across the companyBring OD expertise to assist with the evolution of the culture of the company, preserving positive aspects of current culture and integrating productive changes that are consistent with overall company strategyFacilitate conversations to address organizational issues and drive alignment towards goal-oriented solutionsIdentify key OD metrics and measures that enable effective tracking and monitoring of the overall effectiveness of the organizationMonitor organizational health and respond with appropriate interventionsProvide expertise in organizational design, job design and workforce planningDesign and implement leadership and management development programs, as well as new employment orientationDesign and implement team development and effectiveness programsDevelop training path for key positions in the company, work with managers to establish individual development plans consistent with current job duties and career advancementPlan, organize and lead company-wide employee training programsIdentify, establish and manage effective vendor partnerships to access outsourced OLD resources as neededLeverage external networks and connections to continuously seek best practices and learning to benefit the development of the organizationRequirements:Graduate Degree in Organizational Development or related fieldAt least 10 years’ experience of delivering high impact, practical OD strategies and initiatives in growing organizations, with at least 5 years at a senior levelDeep understanding of organizational development / organizational behavior theories, methods and conceptsStrong, proven organizational consulting skillsExperience leveraging people and organizational data to inform effective OD initiativesWell-developed planning and organization skills, ability to effectively manage multiple prioritiesAbility to think and act with a global mindset, culturally sensitive and awareStrong results orientation with a demonstrated ability to oversee practical, solution-driven initiatives that add value to the businessOutstanding leadership and communication skills (written and verbal) with ability to present views in a clear and compelling manner and develop trust and influence at all levelsExperience with various tools and methods to drive organizational effectivenessPreferred:Pharma or Biotech industry experience Dec 6th, 2021 09:20PM Dec 6th, 2021 09:20PM Arrowhead Research Health Care Pharmaceuticals & Biotechnology
nasdaq:arwr arrowheadpharmaceuticals.applytojob.com arrowheadpharmaceuticals.applytojob.com Dec 7th, 2021 12:00AM Sr. Manager, Regulatory/Medical Writing Open Regulatory Affairs Pasadena CA USA The PositionThe Senior Manager, Regulatory/Medical Writing collaborates with members of cross‑functional teams to prepare high-quality regulatory and clinical documentation for submission to global regulatory agencies including the preparation of components for INDs/NDAs, annual reports, Orphan Drug Designation applications, and briefing books as well as clinical study documentation such as protocols, investigator brochures, etc as required within agreed-upon timelines. The Senior Regulatory/Medical Writer also assists with the preparation of publications, abstracts, and other external communications in support of Arrowhead business functions. The Senior Manager, Regulatory/Medical Writing also assists in implementing processes and standards to ensure company scientific documents are prepared to the highest editorial standards and quality.ResponsibilitiesPrepares, edits, and finalizes protocols, investigator brochures, synopses, clinical study reports, regulatory documents (INDs/NDAs, annual reports, Orphan Drug Designation applications, Agency Response to Questions, briefing books, etc)Prepares related clinical documents, such as abstracts, posters, presentations, and manuscriptsCollaborates with and manages contract medical writers as required for project assignmentsAdvises and assists in the review and management of nonclinical and CMC technical reports as requiredDevelops and maintains company house-standard templates and best review practices for regulatory and clinical documentation; ensure vendors and contractors maintain company standardsParticipates in regulatory and clinical team strategy meetings to ensure that that results and messages in clinical documents accurately reflect the data in tables, figures, and listings (TFLs) and other information sources; partners with the scientific staff including participation in the review of mock and/or blinded TFLs, and narrative planning for relevant documentsAssists in the development and maintenance of Development Core Product Data Sheets, draft labeling, and company work instructions and SOPs, as requestedEnsures that medical writing deliverables conform to International Conference on Harmonization (ICH) and other relevant regulatory guidelines and medical editorial boardsManages the document review process ensuring conflicting and/or ambiguous comments are clarified and appropriately addressed; Schedules and conducts document-related meetings including kickoff meetings and document review planning and alignment discussions to ensure documentation timelines are achievedEnsures documents are generated in accordance with agreed internal processes and standards, are submission ready, and are appropriately stored in appropriate document management system(s)Ensures that appropriate documented quality control (QC) checks are performed on regulatory/medical writing deliverables, responds to findings, and recommends quality process improvementsRequirements:Bachelor’s degree in medically related field or life scienceA minimum of 6 to 8 years of relevant medical writing experience in the pharmaceutical industry is essentialMembership in professional medical writing, regulatory, or drug information associations would be usefulMust have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical research and medical writing standards; demonstrated ability to interpret and apply these guidelines to document writingFamiliarity with basic statistical analysis concepts and techniques A demonstrated track record of contribution to successful regulatory components used in filings eg, IND/CTAs, NDA/BLA/MAAs is importantPrior experience in interacting with cross-functional study team members is essentialHighly proficient in the use of MS Word, Excel, Endnote, Adobe Acrobat, PowerPoint, and structured document templatesPreferred: Post-graduate degree (master’s or doctoral) Experience writing in one or more of the company’s key therapeutic areas eg, liver disease, oncology, or rare diseasesExperience with electronic document management systems is highly desirable Dec 6th, 2021 09:20PM Dec 6th, 2021 09:20PM Arrowhead Research Health Care Pharmaceuticals & Biotechnology
nasdaq:arwr arrowheadpharmaceuticals.applytojob.com arrowheadpharmaceuticals.applytojob.com Dec 7th, 2021 12:00AM Associate Scientist/Scientist, Ophthalmology Lab Open Biology Madison WI USA The Position Arrowhead is seeking an experienced and highly motivated Associate Scientist or Scientist to join our drug discovery team. The individual will be responsible for performing ocular procedures in small animals, operating ophthalmic equipment, analyzing data, and issuing study reports. Requirements: BS or MS in Biology, Physiology, Pharmacology, or a relevant areaMinimum of 2-year experience with delicate procedures or surgery in small animalsExcellent skills of communicationProven capability in rapidly learning new skills and technologyProven capability of multitaskingAbility to coordinate and collaborate with scientists in discovery teamPreferred: Research experience in ocular diseasesExperience in operating imaging and/or electric physiology equipmentKnowledge of ocular physiology Dec 6th, 2021 09:20PM Dec 6th, 2021 09:20PM Arrowhead Research Health Care Pharmaceuticals & Biotechnology
nasdaq:arwr arrowheadpharmaceuticals.applytojob.com arrowheadpharmaceuticals.applytojob.com Dec 7th, 2021 12:00AM Sr. Director, Drug Delivery Open Chemistry Madison WI USA The PositionArrowhead is seeking a Senior Director of Drug Delivery to join the Discovery Chemistry group at our R&D facility located in Madison, WI. This position will be responsible for providing strategic and operational leadership for the development of safe and effective delivery platforms for oligonucleotide. The successful candidate will lead a team of experienced and innovative discovery chemists and biologists, and work cross-functionally with internal departments and external resources.ResponsibilitiesProvide strategic and operational leadership for the research into oligonucleotide delivery and RNAi in new cell typesTrack progress against project plans, generate regular status updates, and communicate progress and issues to managementManage, coach and mentor direct reports, and effectively coordinate team resources to meet aggressive discovery goalsMaintain a continuing knowledge of scientific advances occurring within the industry and academia to keep the cutting edge in the fieldRequirements:Ph.D. in chemistry or chemical biology with a minimum of 12 years of experience of drug delivery research in pharmaceutical industryCreative problem solver with a track record of innovation, preclinical and clinical achievementsExpertise in synthetic chemistry and analytical technology, hands-on experience in syntheses and development of small molecule, peptide or oligonucleotide drug candidatesExcellent communication and interpersonal skills to work in team environmentDemonstrated leadership in team building, team managing and thriving in changesPreferred: Experience in bioconjugation Dec 6th, 2021 09:20PM Dec 6th, 2021 09:20PM Arrowhead Research Health Care Pharmaceuticals & Biotechnology
nasdaq:arwr arrowheadpharmaceuticals.applytojob.com arrowheadpharmaceuticals.applytojob.com Dec 7th, 2021 12:00AM Associate Chemist, CMC Process Development Open Manufacturing Madison WI USA The PositionArrowhead Pharmaceuticals is seeking a highly motivated individual to become a part of its scientific team. We have an immediate opening for an Associate Chemist to work as a Chemist in the Chemistry, Manufacturing, and Controls Group focusing on small molecule process development. This is an ideal position for an individual with an organic chemistry background who has an interest in projects related to novel technology in synthesis and purification of small molecules and bioconjugates. ResponsibilitiesPerform synthesis, purification, and characterization of small molecules with a focus on developing robust proceduresWork closely with senior chemists on development of new synthetic approaches to desired compounds with an eye toward large-scale synthesisCollaborate with other chemists in the group in preparation of complex organic constructsAnalyze small-molecule and macromolecular targets using standard methods Maintain a well-documented laboratory notebookTrack progress against project timelines, generate regular status updates, and communicate progress and issues to management, including presentation of findings at team meetingsCoordinate delivery of materials both internally and externallyRequirements:BS/BA in Chemistry or related field (minimum 1 year of relevant laboratory experienceExperience with synthetic organic chemistryExcellent verbal and written communication skillsStrong problem-solving skillsEagerness to learn new techniquesPreferred:Experience working with both small molecule or large molecule synthetic targets either in an academic or industrial settingBasic familiarity with GLP/GMP regulationsExperience with small-molecule or macromolecule analytical techniques (e.g., HPLC, UV-Vis spectrophotometry, mass spectrometry, NMR, etc.) Dec 6th, 2021 09:20PM Dec 6th, 2021 09:20PM Arrowhead Research Health Care Pharmaceuticals & Biotechnology
nasdaq:arwr arrowheadpharmaceuticals.applytojob.com arrowheadpharmaceuticals.applytojob.com Dec 8th, 2021 12:00AM Associate Director, External Innovation Open Clinical Development Pasadena CA USA The Position Arrowhead is seeking a hands-on, science driven individual to seek out and assess advances in life sciences and chemistry with the potential to enhance Arrowhead’s pipeline of therapeutics. The Associate Director, External Innovation will become the inhouse expert on next generation oligonucleotide and drug delivery technology through review of scientific literature, industry, development updates of relationships with key academics and industry contacts, and other relevant sources. This individual will work with Arrowhead’s cross functional leadership team to evaluate the development path and commercial potential for early stage technologies and identify opportunities for academic and business collaborations, as well as targets for acquisition. The individual will have the opportunity to participate in key business development activities such as licensing and collaboration deals. ResponsibilitiesSystematically collect, track and analyze relevant information at an in-depth technical level through review of scientific publications, industry updates, company updates, conference attendance, and other sourcesInteract with colleagues across R&D, legal, commercial, corporate development and other business functions to gather key information and data to inform areas of technology focusSynthesize findings into relevant insights and continuously improve the research and presentation processDevelop informed perspectives about how findings fit with Arrowhead’s strategic vision.Make regular high quality and efficient presentations to internal and external stakeholders.Maintain dashboards and tracking tools for technologies of interestBuild and maintain strong relationships with key opinion leaders, scientists, innovators and entrepreneurs in both academic and business settingsSupport broader portfolio and business development teams with projects and tasks on an ad-hoc basisRequirements:PhD or advanced degree in Biology, Biochemistry, Chemistry or Biomedical Sciences, or MA/MS in relevant technical field with an MBA5-8 years of experience in pharmaceutical research and developmentExpert technical knowledge in gene-based therapeuticsFamiliarity with landscape of academic and industry participants in areas of company interestAbility to conduct independent, self-directed researchStrong interpersonal and communication skills, including ability to communicate complex technology concepts and technology value proposition to internal and external audiencesStrong oral presentation and written skillsAbility to thrive in a fast-paced, dynamic environment.Demonstrated analytical and creative problem-solving skills.Preferred:Experience in research and development of gene-based therapeutics including RNAi therapeutics, CRISPR or RNA editingTechnology scouting experience Dec 8th, 2021 12:16AM Dec 8th, 2021 12:16AM Arrowhead Research Health Care Pharmaceuticals & Biotechnology
nasdaq:arwr arrowheadpharmaceuticals.applytojob.com arrowheadpharmaceuticals.applytojob.com Dec 8th, 2021 12:00AM Sr. Clinical Research Associate Open Clinical Operations Pasadena CA USA The Position The Sr. Clinical Research Associate (Sr. CRA) provides support to the Clinical Operations Manager (COM)/Study Lead(s) to manage and track key study deliverables. The primary purpose of the position is to support the COM/Study Lead in study set-up, execution, and closeout to ensure study deliverables are met and compliance with clinical protocols, their objectives and ICH and GCP guidelines. This is primarily an in-house role. Responsibilities Support Study Lead to execute study milestones against study timelines   Tracking of key deliverables during start-up, study maintenance and close-out; generate, review and distribute reports from internal tracking at requested intervals (Site Status, Enrollment, Dosing) Collaborate with the Study Lead to develop/review certain study-specific plans and/or processes  Present updates at team meetings as needed (i.e., Clinical Trial Team Meeting, Project Team Meeting, Investigator Meeting, project training, etc.)  Collect and review essential documents from investigational sites Support CTAs with TMF set-up, maintenance, ongoing quality review, and final reconciliation of study documents Participate in study specific tasks such as investigator identification and site activation  Contribute to the development/review of study specific Monitoring Plans; track timing/planning of site visits to ensure compliance Contribute to the development/review of study materials, case report forms (CRFs), informed consent documents for clinical studies Review monitoring visit reports and perform occasional co-monitoring visits with CRO CRAs  Assist in the preparation and review of site reference materials (i.e., screening/enrollment logs, Delegation of Site Responsibilities form, Site Monitoring Log, etc.)  Act as CROs’ CRA/CTA first line of contact for study related questions/issues   Work with the CRO to arrange and prepare for Site Qualification Visits, Site Initiation Visits and Site Investigator Meetings (as applicable)  Provide updates on study/site status as needed to ensure timely study entry and updates are reflected on ClinicalTrials.gov or EU equivalent Assist Study Lead with design and preparation of study related materials for the training of CRO staff  Assist Study Lead with oversight of study vendors (CRO, Drug Supply, Central Lab) as required  Perform remote query and data review as needed to assist CDM  Assist clinical finance and study lead with the review, tracking and management of study specific budgets Required:  4-year college degree (preferred) otherwise, candidates with a combination of education and relevant experience will be considered Minimum of five (5) years in clinical research Minimum of three (3) years onsite monitoring/site management experience Experience managing/supervising vendors Thorough understanding of all applicable FDA ICH- GCP regulations and guidelines Working knowledge of medical terminology Ability to proactively perform and complete duties with minimal supervision in an accurate and timely manner Proficient in MS Office (Word, Excel, and PowerPoint) Ability to work in a team or independently  Effective interpersonal, written and verbal communication skills  Able to critically evaluate job tasks and the impact on overall study execution  Strong problem-solving capabilities  Effectively collaborates with Study Team members  Exceptional organizational skills with the ability to multi-task and prioritize  Attention to detail Ability to work with distributed team members and outside vendors Occasional travel in US or overseas (<10%) Preferred:  CRA certification Dec 8th, 2021 12:16AM Dec 8th, 2021 12:16AM Arrowhead Research Health Care Pharmaceuticals & Biotechnology
nasdaq:arwr arrowheadpharmaceuticals.applytojob.com arrowheadpharmaceuticals.applytojob.com Dec 8th, 2021 12:00AM Recruiter, In House Open Human Resources Pasadena CA USA The PositionAs an in house recruiter with Arrowhead, you will play a key role in helping Arrowhead add to its high performing team. Your primary responsibilities will be to source, screen, interview, and recommend candidates for opportunities within Arrowhead. The position reports to the Vice President, Human Resources and will work closely with hiring managers across Arrowhead in Pasadena, CA, San Diego, CA and Madison, WI.ResponsibilitiesWork with hiring managers to determine necessary skills sets and experiences a candidate must possess in order to be successfulDraft position descriptionsIdentify relevant job posting sites and advertise positionsSource passive candidates with a variety of skill setsIdentify and attend job/career fairs and connect with career services at colleges and universities to promote the companyReview resumes submitted for open positionsPre-screen candidates by phone and in person.Recommend qualified candidates and arrange subsequent interviewsPerform other recruiting related work as assignedRequirements:Bachelor's degree2-4 years’ recruiting experienceDemonstrates proficiency in Microsoft Office and Applicant Tracking Systems and Tools such as recruiting and social/professional mediasExcellent research and communication skillsHighly organized and detail orientedEnjoys working on a computer and in an office settingSelf starter who is motivated to complete and prioritize tasksAbility to manage multiple positionsPreferred: Bachelor's degree in a healthcare or related scientific fieldRecruiting experience for pharmaceutical, biotech or other R&D organizationsSuccessful track record of recruiting for Clinical Operations, Program Management, Pharmacovigilance and/or Regulatory AffairsExperience recruiting for Clinical Data Management, Biostatistics and/or Clinical Programming professionals Dec 8th, 2021 12:16AM Dec 8th, 2021 12:16AM Arrowhead Research Health Care Pharmaceuticals & Biotechnology
nasdaq:arwr arrowheadpharmaceuticals.applytojob.com arrowheadpharmaceuticals.applytojob.com Dec 8th, 2021 12:00AM Animal Technician (Husbandry) Open Animal Facility Madison WI USA The Position: We are seeking an Animal Caretaker to join our Laboratory Animal Resources staff. This is an ideal position for an individual with a background in animal care and husbandry who wants an opportunity to work in a laboratory setting and learn basic animal procedures such as injections and blood draws. Responsibilities Daily observations to assess animal’s general health Cleaning and sanitizing animal areas Monitoring environmental conditions in the vivarium (temperature, humidity, light cycle) Operating cage washer, autoclave, dump and animal transfer stations Housing new arrivals Some computer work (Excel) Placing animal orders Train on basic procedures such as injections and blood draws Good communication skills and ability to work in a team environment Requirements: Ability to lift 50 pounds and extended standing High school diploma or equivalent, some college level education a plus Some overtime and weekend work required Preferred: Experience working with rodents in a laboratory setting a plus Dec 8th, 2021 12:16AM Dec 8th, 2021 12:16AM Arrowhead Research Health Care Pharmaceuticals & Biotechnology

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