FSP Epidemiologist (Japan Data Expertise)

IQVIA; Durham (NC); Remote; USD 110,000 - 277,000; Full time

Job summary

An established industry player is seeking a skilled epidemiologist to design and conduct impactful studies that generate real-world evidence. This role involves collaborating with cross-functional teams and managing stakeholder relationships, all while working remotely. The ideal candidate will possess a PhD in Epidemiology or a related field, with a strong background in observational research methods and data analysis. Join a forward-thinking company dedicated to improving patient outcomes and population health through innovative medical treatments. This is a fantastic opportunity to make a significant impact in the healthcare sector.

Qualifications

• PhD or Master's in Epidemiology with relevant experience in the pharmaceutical industry.
• Expertise in observational research methods and secondary data analysis.

Responsibilities

• Design and conduct epidemiological studies to generate real-world evidence.
• Support development of study protocols and communicate results effectively.

Skills

Epidemiological study design

Statistical analysis

Data source identification

Stakeholder management

Scientific publication

Education

PhD in Epidemiology

Master’s in Epidemiology

Tools

Electronic Health Records (EHR)

Medical claims databases

Job description

Location: Remote, candidates must be US-based

Description:

• Design and conduct epidemiological studies to generate real-world evidence within 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 outcomes, comparative safety and effectiveness research, and post-authorization studies.
• Support the development of study protocols, analysis plans, and study reports to address methodologic questions relevant to RWE.
• Assist in identifying suitable data sources for the timely execution of the RWE strategy.
• Construct cohorts using RWD sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes, planning validation studies as needed.
• Conduct descriptive and comparative analyses for methodologic research questions using RWD.
• Contribute to communicating observational research results and methods, including preparing sections of regulatory documents, reports, publications, and white papers.
• Support effective communication of study and analysis results to inform internal and external decisions.
• Contribute to developing processes and training to enhance the efficiency, quality, and impact of activities.
• Coauthor abstracts and manuscripts for external dissemination of methodologic study findings.
• Demonstrate ability to manage stakeholders, including external vendors and internal cross-functional teams.

Minimum Requirements:

• PhD in Epidemiology or a related field with at least two (2) years of relevant post-doctoral experience, preferably in the pharmaceutical or biotech industry or consulting. Alternatively, a Master’s degree in epidemiology or a relevant scientific field with five (5) years of experience may be acceptable.
• Understanding of observational research methods and experience supporting the design and conduct of such studies, including protocol, analysis plan, and report development.
• Knowledge of secondary data sources and experience with secondary data analysis, especially with electronic medical records and/or medical claims databases.
• Specifically, experience working with Japan claims data and hospital records is required.
• Experience fulfilling post-marketing requirements for the Japanese regulatory agency, Pharmaceuticals and Medical Devices Agency.
• A record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation is preferred.
• Ability to work autonomously and develop productive collaborations in a matrix environment.
• Strong skills in managing priorities and performance targets.
• Ability to attend meetings remotely in Japan time zone approximately 3 times monthly.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other protected status by law. More information is available at https://jobs.iqvia.com/eoe.

The potential base pay range for this role, when annualized, is $110,500 to $276,100. Actual offers may vary based on qualifications, location, schedule, and other factors. Additional incentive plans, bonuses, and benefits may also be offered.