Remote Principal Clinical Data Programmer (SAS/SQL, EDC)

BridgeBio Pharma; San Francisco (CA); Remote; USD 172.000 - 189.000; Vollzeit

Benefits dieser Stelle

Hybrid work expectations

Zusammenfassung

BridgeBio Pharma is seeking a Principal Clinical Database Systems Programmer to design, build, and maintain clinical data collection systems using SAS/SQL. You will develop data listings, reports, and EDC builds while coordinating with biostatisticians and data managers to meet study requirements.

The role emphasizes leadership in data review and standardization across studies, with responsibilities across study data sources, including data from external vendors, and collaboration with

Qualifikationen

• Bachelor's degree in Science and/or IT background.
• 5–7 years in pharma/biotech setting.
• Advanced skills in databases, EDC platforms (Medidata Rave, Veeva), data imports/integrations and data visualization (Tableau, Spotfire).
• Advanced SQL, BASE/SAS, SAS/STAT, SAS MACROS.
• Understanding CDISC/SDTM and ICH GCP.

Aufgaben

• Create standard and custom programs/reports with SAS, SQL, and data visualization tools to support data oversight.
• Lead EDC database build programming including CRFs and edit checks on platforms like Veeva Vault or Medidata Rave.
• Collaborate with statisticians, data managers, and project teams to clarify data specs and ensure data quality.
• Support development and maintenance of data standards, tools, and systems across data sources.
• Manage external data imports and vendor data transfers with Data Management Lead.

Kenntnisse

SQL programming

SAS programming

Python

Data visualization

CDISC/SDTM

Ausbildung

Bachelor's degree

Tools

Medidata Rave

Veeva Vault

Tableau

Spotfire

Jobbeschreibung

BridgeBio Pharma is seeking a Principal Clinical Database Systems Programmer to design, build, and maintain clinical data collection systems using SAS/SQL. You will develop data listings, reports, and EDC builds while coordinating with biostatisticians and data managers to meet study requirements.

The role emphasizes leadership in data review and standardization across studies, with responsibilities across study data sources, including data from external vendors, and collaboration with