Associate Director, Real World Evidence – Pharma Co Experience Required

This is a fully remote position, open to applicants in Arizona, +4 more states.

📋 Description

• This position is available to US employees without the need for sponsorship.

• Work alongside enthusiastic problem solvers, innovating collectively to assist our clients in reaching their objectives.

• Operate with a drug development perspective, leveraging years of experience and extensive expertise to comprehend customer requirements.

• Create cohorts utilizing Real World Data (RWD) sources and assess essential variables.

• Perform analyses for descriptive and comparative research employing RWD.

• Coauthor abstracts and manuscripts for the external dissemination of findings.

⛳️ Requirements

• Experience at PharmaCo is mandatory.

• Developed and implemented study protocols, analysis plans, and reports under Scientific Oversight to address priority research questions in Real World Evidence (RWE).

• Designed and overseen epidemiological, biomarker, and/or data science initiatives.

• Planned, designed, and executed analyses for both internal and external decision-making (such as responses to regulatory bodies and quick assessments of safety inquiries).

• Assisted in identifying suitable data to ensure the timely execution of the RWE strategy.

• Built cohorts using RWD sources (e.g., claims, Electronic Health Records) and evaluate significant variables, including diagnosis and procedure codes, while planning validation studies as necessary.

• Conducted analyses for descriptive and comparative research utilizing RWD (such as claims, EHR, Patient-Reported Outcomes/Clinical Outcome Assessments, registry data) for methodological research inquiries.

• Contributed to the dissemination of observational research results and methodologies, including the development of relevant sections of regulatory documents, reports, publications, and white papers.

• Supported effective communication of study/analysis results to facilitate internal and external decision-making.

• Coauthored abstracts and manuscripts for the external communication of methodological study findings.

• Participated in the development of processes and training focused on enhancing the efficiency, quality, and impact of functional activities.

• Technical expertise in observational research methods (both primary and secondary data collection), in-depth knowledge of biostatistics and analysis techniques, and comprehension of regulatory processes.

• Project implementation experience, including protocol writing, statistical analysis plans, and manuscript and abstract authorship.

🏝️ Benefits

• Company car or vehicle allowance.

• Comprehensive health benefits, including Medical, Dental, and Vision coverage.

• Company-matched 401(k) plan.

• Eligibility to enroll in the Employee Stock Purchase Plan.

• Opportunity to earn commissions and bonuses based on individual and company performance.

• Flexible paid time off (PTO) and sick leave.