Associate Director overseeing evidence generation projects for cancer treatments at Genmab. Focus on managing programs, compliance, and collaborating across teams in a hybrid work environment.
Responsibilities
Execute plans with great technical depth and breadth (training & compliance, project management, medical education, grants & sponsorships)
Define work instructions/process flows within own area/study
Implement delivery plans and provide periodic reporting in line with overall CoE strategy (e.g. project metrics, training outcomes, grant outcomes, budgets, vendor metrics)
Guide cross-functional and direct team members to drive compliance and address issues related to deliverables
Actively contribute in teams and meetings, collaborate with other medical affairs groups and external stakeholders as required
Train and mentor others around new technologies and scientific aspects of applied scientific research
Oversee successful implementation of Investigator-Driven programs
Successfully develop, implement, and manage 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 implements solutions to achieve project goals
Participate in process improvement exercises to drive operational excellence.
Requirements
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.
Benefits
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
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