Director, Global Medical Affairs (Oncology)
About The Position
The Medical Lead, Global Medical Affairs Oncology has a key role in the Global Medical Affairs Oncology team and works closely with partners internally in the medical team, as well as with other R&D functions such as clinical development, pharmacovigilance, regulatory affairs, preclinical and translational research, PKPD, publications and program management. This role works within the cross-functional team responsible for the development and life cycle management of one of our cancer therapies. Responsibilities include working closely with his/her management and other Medical Directors of the Global Medical Affairs Oncology team to build, monitor, track, manage, and assist with the development and implementation of the Global Medical Affairs plans and initiatives.
Requirements
- Advanced science degree: MD or PhD, with experience in oncology (required)
- Minimum of 5 years of experience in the pharmaceutical/healthcare industry, or equivalent academic experience with demonstration of successful results
- Demonstrated understanding of drug development and experience with phase 1 to phase 3 trials
- Strong global medical affairs experience, including medical affairs strategic planning and execution of tactical initiatives (minimum 3 years)
- Knowledge and application of business planning & leadership principles, such as goal setting, action plans, monitoring tools, directive, and supportive techniques to develop and implement action plans
- Demonstrated ability to work with teams, manage a diverse work group, motivate them, and maximize productivity
- Creation and oversight of cross-functional and multi-disciplinary teams
- Possess budget experience and knowledge
- Experience in working in a team in a matrix structure in changing a competitive environment, changing product technology, and changing needs
- Demonstrated orientation & credibility with internal and external customers
- Creation of solid plans and reports for which performance and progress can be measured and evaluated
- English - excellent command of spoken and written English (German a plus)
- High integrity and work ethics
- Adaptability and ability to remain focused in the presence of shifting priorities and strategies in a timely response to the business climate
Nice To Haves
- German a plus
Responsibilities
- Support the acceleration of BioNTech's clinical trials.
- Advance scientific knowledge
- Communicate scientific data and educate healthcare professionals
- Identify and bring awareness to impactful medical insights and strategic planning
- Collaborate with stakeholders to transform cancer care to improve the lives of patients with cancer by driving innovation in the field of immuno-oncology.
Benefits
- Medical, Dental and Vision Insurance
- Life, AD&D, Critical Illness Insurance
- Pre-tax HSA & FSA, DCRA Spending Accounts
- Employee Assistance & Concierge Program (EAP) available 24/7
- Parental and Childbirth Leave & Family Planning Assistance
- Sitterstream: Virtual Tutoring & Childcare Membership
- Paid Time Off: Vacation, Sick, Bereavement, Holidays (including Floating) & Year-End U.S. Shutdown.
- 401(K) Plan with Company Match
- Tuition Reimbursement & Student Loan Assistance Programs
- Wellbeing Incentive Platforms & Incentives
- Professional Development Programs
- Commuting Allowance and subsidized parking
- Discounted Home, Auto & Pet Insurance
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What This Job Offers
Job Type
Full-time
Career Level
Director
Industry
Chemical Manufacturing
Education Level
Ph.D. or professional degree
Number of Employees
1,001-5,000 employees
