Principal Clinical Data Systems Programmer (Remote)

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

Benefits offered by this job

Market-leading compensation

401(k) with employer match

Employee Stock Purchase Program (ESPP)

Hybrid work model with flexibility

Flexible, take-what-you-need paid time

Job summary

BridgeBio seeks a Principal Clinical Database Programmer to design, build, and maintain clinical data collection systems. You will develop data listings and reports, lead EDC builds, and collaborate with biostatisticians on study data structures.

Responsibilities include data standardization, tool development, and vendor liaison for data transfers. A PhD/BS in science or IT is preferred with 5–7 years in pharma/biotech.

Qualifications

• Bachelor’s degree (or equivalent) in Science and/or Computer Systems/IT background.
• Minimum 5-7 year experience in a pharmaceutical/biotech setting.
• Advanced technical expertise in databases, EDC platforms (e.g. Medidata Rave, Veeva), data imports/integrations and data visualization tools (e.g. Tableau, Spotfire) and Python programming language is a plus.
• Advanced programming and analytical skills using SQL, BASE/SAS, SAS/STAT, SAS MACROS.

Responsibilities

• Creates standard and/or custom programs/reports using data analytics tools such as SAS, Tableau, or other data visualization tools to support data oversight and review by data managers or other data reviewers.
• Leads EDC database build programming, testing, and migration of CRFs and edit checks or dynamics (database specifications, etc.) using EDC platforms (e.g. Veeva Vault, Medidata Rave).
• Collaborates with clients, peers, programmers, project teams, and/or requestors to clarify and finalize data specifications; uses expanded technical skills to meet evolving project needs.
• Supports the development, delivery and maintenance of clinical data review standards, tools and systems, across various data sources (e.g., clinical data, safety and operational data).
• Supports initiatives for Data Management and Clinical Programming for clinical data review bridging and database development activities, meetings, discussions.
• Assists in the management of electronic data from external data sources/vendors in partnership with the Data Management Lead for import or integration to clinical database tools. Liaises with vendors as needed to facilitate electronic data transfers and/or data specification requirements.
• Assists in review and approval of required study documentation, including design specifications, user requirements, data transfer specifications and data standards.
• Provides leadership, training, guidance, and support to other department members on data review tools and clinical database development.

Skills

SQL

BASE/SAS

SAS/STAT

SAS MACROS

Python

Data visualization

Education

Bachelor’s degree in Science/IT

Tools

Medidata Rave

Veeva Vault

Tableau

Spotfire

Job description

BridgeBio seeks a Principal Clinical Database Programmer to design, build, and maintain clinical data collection systems. You will develop data listings and reports, lead EDC builds, and collaborate with biostatisticians on study data structures.

Responsibilities include data standardization, tool development, and vendor liaison for data transfers. A PhD/BS in science or IT is preferred with 5–7 years in pharma/biotech.