Senior Director – RWE/Epi Breast Oncology Team Lead
Company | Pfizer |
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Location | Cambridge, MA, USA, Boston, MA, USA, San Francisco, CA, USA, Tampa, FL, USA, Bothell, WA, USA, Phoenixville, PA, USA, La Jolla, San Diego, CA, USA, Groton, CT, USA, New York, NY, USA |
Salary | $219800 – $366400 |
Type | Full-Time |
Degrees | Master’s, PhD |
Experience Level | Senior, Expert or higher |
Requirements
- Advanced degree, including PhD in Epidemiology, population health, outcomes research, or a related discipline and 7+ years of relevant experience in the pharmaceutical, academic and/or medical environments (at least 3 of which need to be at a pharmaceutical company or partnering with pharmaceutical companies); or, MPH or another relevant Master’s degree, and 10+ years of experience with similar requirements as previously stated.
- Proven leader of effective teams/individuals and has a track record of fostering colleague growth.
- Experience operating within large cross-functional matrices and collaborating with multiple partners.
- Strong technical expertise, analytic ability, creative problem-solving, and communication skills.
- Experience directing analyses of real-world data, which would include Flatiron Health or similar.
- Proven hands-on experience leading and executing non-interventional (NI) studies from protocol design, delivery of results and clinical study report.
- Knowledgeable of the external regulatory environment for real-world evidence and maintains awareness of scientific developments in epidemiology, medicine, and technology (e.g., artificial intelligence).
- Educational and/or work experience supporting Oncology RWE/Epi studies, particularly Breast Oncology.
Responsibilities
- Oversee team execution of real-world evidence and epidemiology studies as part of cross-functional Integrated Evidence Plans.
- Design, lead and execute real-world evidence and epidemiology studies as part of cross-functional Integrated Evidence Plans.
- Provide subject matter expertise and thought leadership to advance Pfizer’s use of RWE/Epi to develop high value medicines.
- Partner with TA RWE/Epi lead and MEG TA Leads to ensure strategic input is being provided to IEPs through Global Medical Affairs Teams.
- Work collaboratively to establish & operationalize processes & systems to deliver RWE/Epi studies and other deliverables to execute on IEP plans.
- Stakeholder management: build coalitions & develop strong partnerships across disciplines & geographies to optimize RWE/Epi team’s performance / contribution.
- Provide critical assessment to inform asset-specific development strategy & cross-functional decision-making and review of epidemiological data and literature, when needed.
- Prepare study reports, and present /publish results of epidemiological studies at scientific conferences and in peer-reviewed journals.
- Participate in RWE/Epi peer review of study protocols and study reports.
Preferred Qualifications
- At least 3 years of experience leading and managing a team.
- Proven hands-on experience leading and executing NI PASS studies from protocol design, delivery of results and clinical study report.
- Ability to develop and implement strategic plans and business objectives.
- Strong problem-solving skills and the ability to influence senior leadership.
- Educational and/or work experience leading and executing Breast Oncology RWE/Epi studies.
- Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.