Lead Clinical Data Systems Programmer - Remote

bridgebio; United States; Remote; USD 172,000 - 189,000; Full time

Benefits offered by this job

Remote work (US-based)

Office visits in San Francisco

Medical, dental, vision coverage

Retirement matching

Paid leave & PTO

Professional development

Job summary

BridgeBio seeks a Lead Clinical Database Programmer to design, implement, and oversee clinical data systems across studies. You will program databases, listings, reports, and visualizations using SQL or SAS, and ensure quality through testing and validation.

Ideal candidates have 5–7 years in pharma/biotech, hands-on experience with Medidata Rave or Veeva, and strong CDISC/SDTM knowledge. This US-based remote role includes SF office visits and comprehensive benefits.

Qualifications

• Bachelor’s degree or equivalent in science, computer systems, or information technology.
• 5–7 years of experience in pharmaceutical or biotechnology settings.
• Advanced programming and analytical skills with SQL and SAS, including BASE/SAS, SAS/STAT, and SAS macros.
• Experience with clinical databases and EDC systems such as Medidata Rave or Veeva; ability to create datasets, edit checks, and data review outputs.
• Understanding of CDISC and SDTM requirements, including standard datasets creation and validation.
• Knowledge of ICH Good Clinical Practice and Good Clinical Data Management guidelines.

Responsibilities

• Build and maintain clinical data systems, including study databases, programmed listings, reports, and visualizations using SQL or SAS and related tools.
• Lead electronic data capture database programming, testing, and migration of CRFs, edit checks, and database configurations.
• Clarify study specifications with project partners and translate requirements into reliable programming and data structures.
• Develop and maintain standards, tools, and systems for reviewing clinical, safety, and operational data.
• Coordinate external data imports and integrations with data management leads and vendors; support transfer specifications.
• Review study documentation such as design specifications, user requirements, data transfer specifications, and data standards.
• Provide technical guidance and training to colleagues working on clinical database development and data review tools.

Skills

SQL

SAS

BASE/SAS

SAS/STAT

SAS macros

Medidata Rave

Veeva

CDISC/SDTM

ICH GCP

Python

Education

Bachelor’s degree in science / IT

Tools

Medidata Rave

Veeva

Job description

BridgeBio seeks a Lead Clinical Database Programmer to design, implement, and oversee clinical data systems across studies. You will program databases, listings, reports, and visualizations using SQL or SAS, and ensure quality through testing and validation.

Ideal candidates have 5–7 years in pharma/biotech, hands-on experience with Medidata Rave or Veeva, and strong CDISC/SDTM knowledge. This US-based remote role includes SF office visits and comprehensive benefits.