Genmab
Associate Director, Evidence Generation
Genmab –
Copenhagen, Denmark; Utrecht, Netherlands; Princeton, NJ, USA
The Associate Director, Evidence Generation will play a key role in executing Medical Affairs Evidence Generation projects for both approved and pipeline products. This position will be responsible for overseeing a molecule program as well as performing operational aspects of Investigator‐Driven Programs (e.g., Investigator‐Sponsored trials, Collaborative Research Trials, Managed Access Programs).
Responsibilities
Oversee successful implementation of investigator‐driven programs.
Execute formal review process for proposals, protocols, and amendments.
Facilitate review committee meetings and document decisions.
Drive operational timelines and key deliverables for the program or project.
Manage proposal lifecycle from submission to study closure.
Provide guidance and oversight for the successful management of all aspects of investigator‑driven programs within designated program budgets and timelines.
Partner with cross‑functional teams and alliance partners to manage, adjust, and revise project timelines/budgets as necessary.
Generate regular metrics and reports of program activities and present them to leadership and strategy team as needed.
Support field‑based teams and MASL teams in executing project/program goals.
Work cross‑functionally with internal teams which may include development, research, legal, finance, supply chain, and regulatory.
Independently manage ISTs including site coordination, document management, and drug shipment and payments.
Contribute to contract review and negotiations.
Communicate project status and issues and ensure project team goals are met.
Represent the department at cross‑departmental events, as needed.
Functional expertise to initiate, author, or contribute to SOP development, implementation, and training.
Anticipate moderately complex obstacles and client difficulties and implement solutions to achieve project goals.
Ability to resolve problems using national and international regulations, guidelines, and investigator interactions.
Participate in process improvement exercises to drive operational excellence.
Qualifications
Bachelor's or Master's or Advanced degree in a scientific discipline.
8+ years of relevant experience in pharma/biotech industry, preferably in Oncology.
Program and/or Project management experience with leading teams, study protocols or programs preferred.
Experience managing global ISTs and/or Medical Affairs initiatives preferred.
Therapeutic knowledge in oncology (e.g., lymphoma, breast cancer, solid tumors), pharma and biologics is a plus.
Experience with budgeting and contracting.
Experience producing and analyzing metrics/reports.
High attention to detail, strong analytical and organizational skills.
Excellent ability to prioritize workload.
Demonstrated ability to efficiently assimilate diverse and complex medical and scientific data from sponsored or independent non‑clinical and clinical studies and articulate summary information in verbal and written form.
Salary Range – United States $171,360.00 – $257,040.00
Benefits (U.S. Employees)
401(k) Plan: 100% match on the first 6% of contributions.
Health Benefits: Two medical plan options (including HDHP with HSA), dental and vision insurance.
Voluntary Plans: Critical illness, accident, and hospital indemnity insurance.
Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave.
Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well‑being support.
Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses.
Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard‑working, innovative and collaborative team has invented next‑generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T‑cell engagers, antibody‑drug conjugates, next‑generation immune checkpoint modulators and effector function‑enhanced antibodies.
Genmab 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
Genmab.com
and follow us on LinkedIn and X.
#J-18808-Ljbffr
Copenhagen, Denmark; Utrecht, Netherlands; Princeton, NJ, USA
The Associate Director, Evidence Generation will play a key role in executing Medical Affairs Evidence Generation projects for both approved and pipeline products. This position will be responsible for overseeing a molecule program as well as performing operational aspects of Investigator‐Driven Programs (e.g., Investigator‐Sponsored trials, Collaborative Research Trials, Managed Access Programs).
Responsibilities
Oversee successful implementation of investigator‐driven programs.
Execute formal review process for proposals, protocols, and amendments.
Facilitate review committee meetings and document decisions.
Drive operational timelines and key deliverables for the program or project.
Manage proposal lifecycle from submission to study closure.
Provide guidance and oversight for the successful management of all aspects of investigator‑driven programs within designated program budgets and timelines.
Partner with cross‑functional teams and alliance partners to manage, adjust, and revise project timelines/budgets as necessary.
Generate regular metrics and reports of program activities and present them to leadership and strategy team as needed.
Support field‑based teams and MASL teams in executing project/program goals.
Work cross‑functionally with internal teams which may include development, research, legal, finance, supply chain, and regulatory.
Independently manage ISTs including site coordination, document management, and drug shipment and payments.
Contribute to contract review and negotiations.
Communicate project status and issues and ensure project team goals are met.
Represent the department at cross‑departmental events, as needed.
Functional expertise to initiate, author, or contribute to SOP development, implementation, and training.
Anticipate moderately complex obstacles and client difficulties and implement solutions to achieve project goals.
Ability to resolve problems using national and international regulations, guidelines, and investigator interactions.
Participate in process improvement exercises to drive operational excellence.
Qualifications
Bachelor's or Master's or Advanced degree in a scientific discipline.
8+ years of relevant experience in pharma/biotech industry, preferably in Oncology.
Program and/or Project management experience with leading teams, study protocols or programs preferred.
Experience managing global ISTs and/or Medical Affairs initiatives preferred.
Therapeutic knowledge in oncology (e.g., lymphoma, breast cancer, solid tumors), pharma and biologics is a plus.
Experience with budgeting and contracting.
Experience producing and analyzing metrics/reports.
High attention to detail, strong analytical and organizational skills.
Excellent ability to prioritize workload.
Demonstrated ability to efficiently assimilate diverse and complex medical and scientific data from sponsored or independent non‑clinical and clinical studies and articulate summary information in verbal and written form.
Salary Range – United States $171,360.00 – $257,040.00
Benefits (U.S. Employees)
401(k) Plan: 100% match on the first 6% of contributions.
Health Benefits: Two medical plan options (including HDHP with HSA), dental and vision insurance.
Voluntary Plans: Critical illness, accident, and hospital indemnity insurance.
Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave.
Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well‑being support.
Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses.
Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard‑working, innovative and collaborative team has invented next‑generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T‑cell engagers, antibody‑drug conjugates, next‑generation immune checkpoint modulators and effector function‑enhanced antibodies.
Genmab 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
Genmab.com
and follow us on LinkedIn and X.
#J-18808-Ljbffr