Associate Director, Global Drug Safety & Pharmacovigilance Scientist

At Genmab, we are dedicated to building extra[not]ordinaryu
00ae futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicinesu
00ae that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.

Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.

Does this inspire you and feel like a fit? Then we would love to have you join us!

Genmab is an international biotechnology company specializing in the invention and development of differentiated human antibody therapeutics for the treatment of cancer and other important human diseases.

Genmab is on an ambitious growth path and to support this growth Genmab is looking for an additional Global Drug Safety (DS) and Pharmacovigilance (PV) Scientist to join the team in Princeton.

As an Associate Director of Drug Safety and Pharmacovigilance, 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 Safety colleagues along with cross-functional team members. This position has a global perspective, and you will interact with stakeholders ranging from regulatory authorities and colleagues from Genmab’s four sites.

As an Associate Director of Drug Safety and Pharmacovigilance you will be part of a highly skilled and international team. The position reports to the Director, Global Drug Safety & Pharmacovigilance, Scientist Lead.

• Contribute to the development of safety strategy and safety deliverables for assigned programs for assigned programs in close collaboration with key stakeholders from GDS&PV and other cross functional teams
• Perform ongoing surveillance (including signal detection/evaluation) of Genmab clinical trials and post marketing safety data
• Be the primary safety contact for other departments and ensure appropriate and timely handling of safety issues for assigned trials/programs
• Provide safety review and input to various documents including but not limited to:
  Trial Protocols, eCRFs/CRFs, and TMFs
• You will also be contributing to the development ofother documentation such as:
  Investigator’s Brochures, and Subject Informed Consent
• Contribute to HA requests and review key submission documents
• Contribute to safety-related documents for Genmab products throughout product lifecycle from FIH to post-marketing, including robust safety surveillance, Safety Assessment Reports for potential signals/risks, RSI in IB, ADR in the CCDS and product labels, Aggregate Safety Reports (e.g. DSUR, PBRER, PSUR, PAER), RMP, and responses to ad-hoc requests for safety information internally and externally
• Contribute to the planning and conduct of Safety Committee activities and DMC’s
• Conduct safety training of Genmab employees, CROs, Investigators and other relevant site personnel as necessary
• Contribute to multidisciplinary project groups including membership of the Clinical Management Team (CMT) for assigned products
• Contribute to the development and optimization of new tools and process
• Contribute to multidisciplinary project groups including membership of the Clinical Management Team (CMT) for assigned products
• Interact with safety and clinical CROs,…