Senior Manager, MED Oncology RWE/Epi Scientist

This is a fully remote position, open to applicants in Poland.

📋 Description

• Assist in real-world evidence and epidemiologic studies as part of the Medical strategy throughout the entire drug development lifecycle.

• Integrate literature findings and aid in the design, execution, and reporting of global epidemiologic research studies concerning Pfizer Oncology pipeline assets and approved products.

• Ensure the quality, timeliness, and effectiveness of RWE/Epi deliverables within the designated product/disease area.

• Foster an internal network of Pfizer stakeholders to promote innovation, enhance cross-functional collaboration, and identify new RWE/Epi opportunities.

• Establish external partnerships to utilize data resources and collaborate on high-priority global studies.

• Write and review study protocols, reports, and presentations.

• Communicate effectively in writing and presentations with internal stakeholders, regulatory bodies, and medical professionals.

• Provide non-study outputs such as RWE insights, epidemiology literature reviews, regulatory responses, and departmental initiatives.

• Collaborate with Chief Medical Office colleagues to fulfill asset-team evidence requirements and assist in global regulatory submissions to the FDA, EMA, and other agencies.

• Generate rapid insights from real-world observational data sources.

• Create presentations, webinars, manuscripts, scientific data packages, and other communication materials.

• Ensure quality, compliance, and oversight of research activities.

• Engage in peer review of RWE/Epi study protocols and reports.

• Document requests and monitor progress towards project completion, metrics, and business objectives.

• Report directly to the Oncology Team Lead in RWE/Epi.

⛳️ Requirements

• PhD in Epidemiology, Statistics/Biostatistics, Health Outcomes Research, Quantitative Methods, Public Health, Health Economics, or another biological science field with a significant quantitative aspect, along with a minimum of 1 year of pertinent experience in a pharmaceutical, academic, and/or medical setting; or an MPH or another relevant Master’s degree with at least 5 years of experience in the pharmaceutical, academic, and/or medical environment, including at least 1 year in the pharmaceutical industry.

• Proficient quantitative skills and methods expertise for deriving rapid insights from real-world/observational data sources.

• Excellent technical writing and oral presentation abilities, with a proven history of publishing in peer-reviewed journals and presenting at medical/scientific conferences.

• Capability to transform complex analyses into actionable insights using data visualization and presentation tools.

• Proficient in manipulating and analyzing complex structured and unstructured data from various real-world evidence sources.

• Ability to perform under pressure with a high degree of autonomy and leadership on research projects.

• Capacity to collaborate with multiple partners within a matrixed environment.

• Understanding of the external regulatory landscape for real-world evidence.

• Knowledge of scientific advancements in epidemiology, medicine, and technology, including artificial intelligence.

🏝️ Benefits

• Flexible workplace culture that promotes work-life balance.

• Support for reasonable adjustments and disability inclusion.

• Equal employment opportunities.

• A patient-centric, values-driven workplace culture.