Job Description:
We are looking for an experienced professional to support real-world evidence (RWE) initiatives. The role requires a doctoral degree in Epidemiology or a closely related field, with a minimum of three years of hands-on experience in observational research. Responsibilities will include preparing study concepts, maintaining tracking tools, and acting as a representative for RWE in cross-functional groups. Candidates should be proficient in communicating complex findings clearly and may find an advantage in familiarity with SAS or R.
Responsibilities:
Design and execute observational studies using healthcare databases such as claims, EHR, registries, and other secondary data sources.
Develop study protocols, statistical analysis plans (SAPs), and technical documentation for RWE projects.
Conduct data analysis, interpretation, and quality review to ensure scientific accuracy and compliance with study objectives.
Collaborate with biostatistics, clinical, medical affairs, regulatory, and commercial teams to support evidence-generation strategies.
Support publication activities, including abstracts, manuscripts, posters, and conference presentations.
Evaluate data sources and study feasibility for research questions related to safety, effectiveness, and health outcomes.
Ensure adherence to regulatory and industry guidelines, including pharmacoepidemiology best practices and data privacy requirements.
Present study findings and recommendations to internal stakeholders and external partners in a clear, concise manner.
Monitor advancements in real-world data (RWD), epidemiologic methods, and healthcare analytics to improve research quality.
Assist in vendor management and coordination with external research partners/CROs for study execution and deliverables.
