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 for US employees who do not require sponsorship.

• Work in collaboration with enthusiastic problem solvers, innovating as a team to assist our customers in achieving their objectives.

• Approach tasks with a drug development mindset, utilizing extensive experience and profound knowledge to comprehend customer requirements.

• Build 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 communication of findings.

⛳️ Requirements

• Experience with PharmaCo is essential.

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

• Designed and supervised epidemiological, biomarker, and/or data science projects.

• Planned, designed, and executed analyses for both internal and external decision-making (e.g., responses to regulatory bodies, urgent safety analysis).

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

• Created cohorts using RWD sources (e.g., claims, Electronic Health Records) and assessed key variables, including diagnosis and procedure codes, while preparing validation studies as necessary.

• Conducted analyses for descriptive and comparative research using 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 for regulatory documents, reports, publications, and white papers.

• Supported the clear communication of study and analysis outcomes to facilitate internal and external decision-making.

• Coauthored abstracts and manuscripts for the external dissemination of methodological study results.

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

• Technical Proficiency: Knowledge of observational research methods (both Primary and Secondary Data Collection), extensive understanding of biostatistics and analysis techniques, and familiarity with regulatory processes.

• Project Execution: Involvement in protocol writing, Statistical Analysis Plans (SAP), and the creation of manuscripts and abstracts.

🏝️ Benefits

• Company car or car allowance.

• Health benefits including Medical, Dental, and Vision coverage.

• Company-matched 401k.

• Eligibility to participate in the Employee Stock Purchase Plan.

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

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