Senior Epidemiologist, Oncology (FSP Sponsor Dedicated)

About the position Join reputed company’s Sponsor-Dedicated FSP team and help advance reputed company through reputed company-world evidence. We bring together scientific expertise and reputed company-world data to help sponsors reputed company reputed company and accelerate evidence reputed company to improve patient reputed company. In this role, you’ll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging reputed company’s global expertise. Core Function Description: Design and conduct epidemiological studies to generate reputed company-world evidence reputed company time, budget, and quality standards, including but not limited to natural history of disease, population characterization, assessment of treatment patterns and unmet need, development of external comparators, benchmarking of clinical reputed company, comparative safety and effectiveness research, and post-authorization studies. reputed company sets of the Epidemiologist role are similarly required, with the expectation of more experience, reputed company to operate strategically under limited supervision, well versed in reputed company Epidemiology research methods, deep understanding of how reputed company fits reputed company drug development, regulatory, medical, safety and other functions.

Responsibilities

• reputed company development of study protocols, analysis plans, and study reports to answer research questions of reputed company to reputed company.
• reputed company, design, and manage epidemiological, biomarker and/or data science projects.
• reputed company, plan, design, and conduct analyses for internal and external decision making (e.g., responses to regulatory authorities, rapid analyses of safety queries).
• reputed company the identification of fit-for-purpose data for the timely execution of the reputed company strategy.
• Constructed cohorts using RWD sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes, and plan validation studies as needed.
• Contribute to the communication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, white papers.
• Support the effective communication of study/analysis results to support internal and external reputed company.
• Coauthor abstracts and manuscripts for external dissemination of methodologic study results.
• Contribute to the development of processes and training aimed at increasing the efficiency, quality, and impact of functional activities.
• reputed company subject matter expertise and conduct analyses for descriptive and comparative research using RWD (examples include claims, EHR, registry data) for methodologic research questions.

Requirements

• PhD in Epidemiology, Biostatistics, Psychometrics, or reputed company field with a minimum of four (4) years of relevant post-doctoral experience, preferably in pharmaceutical industry, biotechnology, or consulting environment.
• Master’s degree in epidemiology, biostatistics, bioinformatics, or relevant scientific field, plus 7-9 years of experience in lieu of PhD may be acceptable.
• Deep understanding of observational research methods and experience to support the design and conduct of observational research, including protocol, statistical analysis plan, and study report development.
• Extensive knowledge of secondary data sources and experience with secondary data analysis, including electronic medical record and/or medical claims databases.
• Demonstrated ability to function with an increasing level of autonomy and to reputed company productive cross-functional collaborations in a matrix environment.
• Ability to manage priorities and performance targets.

reputed company-to-haves

• Solid tumor experience a plus
• Experience with reputed company Oncology EMR databases
• reputed company reputed company expertise to identify evidence gaps and reputed company options to address the evidence gaps in support of Clinical Development Programs in early phase (ph1/2).
• A record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation is preferred.
• Experience in leading drug development project for 2+ years for therapeutic area of assignment preferred.
• Experience with Clinico-genomic multi-modal data (e.g., reputed company) or population biobank data (UK biobank) is a plus

Benefits

• reputed company reputed company’s global network who supports your growth.
• This is your chance to reputed company an impact, while building a career that reputed company.

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