Job Description

As a member of the CDS-RWE Analytics group, the RWD Analyst reports directly Head of RWE Analytics and is responsible for the design and conduct of statistical analyses of RWD to assess the value of Gilead therapies and perform data visualization and QCs TFLs to communicate results to internal stakeholders in Real World Evidence. The RWD Analyst will align with the Real-World Evidence Therapeutic Area (TA)-aligned Lead to conduct timely, relevant, and rigorous analysis of RWD to address critical research questions, as well as collaborate with CDS to develop, refine, and scale data management and analytic procedures, systems, workflows, best practices, and other issues.

Key Responsibilities

• Develop and QC TFLs for protocols/reports/manuscripts from RWE research conducted to assess the value of the client's therapies using RWD (e.g. claims and EHR).
• QC programming for descriptive and complex studies using RWD.
• Conduct analyses and develop specifications for descriptive and complex statistics in studies using RWD.
• Write the statistical analysis plan (SAP) for descriptive and complex studies using RWD, including from internal client-sponsored prospective cohort studies, claims, charge master and EHR in collaboration with RWE TA lead
• Understand methods and programming to support Comparative Effectiveness Research (CER) analyses, as well as analyses of patient-reported outcomes (PRO) or other patient outcome data
• Develop and QC TFLs for protocols/reports/manuscripts from RWE research conducted to assess the value of our client's therapies using RWD (e.g. claims and EHR)
• Work with RWE researchers to generate code lists for new measures in RWD

Knowledge, Skills and Experience

• Masters degree (e.g. MA, MSc, MPH) in Biostatistics, Epidemiology or related discipline, such as Outcomes Research from an accredited institution, with a minimum of eight (8) years of relevant, post-graduation experience.
• Doctoral level training with a minimum of two (2) years of relevant experience is preferred. Direct experience in lieu of academic training is acceptable.
• Knowledge of real-world data and experience in observational research study design, execution and communication.
• Strong track record of analysis of a broad range of RWD.
• Formal training in Programming and demonstrated proficiency in statistical analysis programs commonly used in life sciences (e.g. SAS, R).
• Understanding of epidemiology or outcomes research and the application of retrospective or prospective studies to generate value evidence.
• Ability to effectively communicate statistical methodology and analysis results.
• Ability to work effectively in a constantly changing, diverse, and matrix environment.
• Knowledge of US secondary data sources required; additional experience with international data sources is preferred.
• Knowledge and experience in qualitative analysis and data sets (e.g., free-text natural language processing, survey data) is preferred.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science

• Industries

  Hospitals and Health Care and Pharmaceutical Manufacturing

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Inferred from the description for this job

Vision insurance

Medical insurance

401(k)

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