Principal Clinical Database Systems Programmer
Bridgebio · Remote - USA
About this role
**Mavericks Wanted** If you’re someone who defies convention, join BridgeBio and help reengineer the future of biopharma—using curiosity, experimentation, and the ethical, thoughtful use of AI to improve clarity, speed, and quality. --- ## What You’ll Do The **Principal Clinical Database Systems Programmer** will perform **SAS or SQL data programming** to design, build, and maintain **clinical data collection systems**. This includes: - Developing **customized data listings** and **data reports/visualizations** - Supporting **EDC study database builds** - Managing **study-defined specifications and requirements** to lead clinical programming activities across one or more studies - Liaising with **biostatisticians** to understand final requirements and structure of study data/database design --- ## Responsibilities - Create **standard and/or custom programs/reports** using tools such as **SAS, Tableau**, or other visualization platforms to support data oversight and review - Lead **EDC database build programming**, including **testing** and **migration** of CRFs and edit checks/dynamics (e.g., database specifications) using platforms such as **Veeva Vault** or **Medidata Rave** - Collaborate with clients, peers, programmers, and project teams to clarify and finalize **data specifications** - Support development, delivery, and maintenance of **clinical data review standards, tools, and systems** across data sources (clinical data, safety, operational data) - Support Data Management/Clinical Programming initiatives for clinical data review bridging and database development activities - Assist with management of electronic data from external sources/vendors for **import/integration** into clinical database tools; coordinate with vendors for transfers and specifications - Assist in review/approval of study documentation including **design specifications**, **user requirements**, **data transfer specifications**, and **data standards** - Provide **leadership, training, guidance, and support** to others on data review tools and clinical database development --- ## Where You’ll Work - **U.S.-based remote** role - Requires **quarterly (or as needed) visits** to the **San Francisco office** - **< 10% travel** anticipated (conferences, Biometrics/DM meetings, BBIO events) --- ## Who You Are - **Bachelor’s degree** (or equivalent) in Science and/or Computer Systems/IT background - **5–7+ years** experience in a **pharmaceutical/biotech** setting - Advanced expertise in **databases**, **EDC platforms** (e.g., Medidata Rave, Veeva), **data imports/integrations**, and visualization tools (e.g., **Tableau**, Spotfire); **Python** is a plus - Strong programming/analytical skills using **SQL**, **BASE/SAS**, **SAS/STAT**, **SAS macros** - Ability to work independently to create standard datasets, program edit checks, and produce quality data review outputs - Demonstrated understanding of **CDISC** and **SDTM** requirements and ability to create/validate CDISC standard datasets - Knowledge of **ICH GCP** and Good Clinical Data Management guidelines - **< 10% travel** as required --- ## Salary (California) **$172,000 – $188,600 USD** (anticipated range for candidates working in California). Final offer depends on experience, education, location, and interview performance. --- *BridgeBio offers a market-competitive total rewards package including base pay, annual performance bonus, company equity, and generous health benefits. Benefits may vary
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