Principal Database Programmer Lisboa

Overview

Join to apply for the Principal Database Programmer role at TFS Health
Science

TFS Health
Science is a leading global
- size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes
- service capabilities, resourcing, and Functional Service (FSP) solutions.

We are currently looking for a Principal Database Programmer. This is a key role responsible for leading and executing database programming activities to support clinical studies, ensuring quality, compliance, and operational excellence.

Key Responsibilities

• Provide training and mentoring to (Senior) Database Programmers on CDMS systems and processes
• Plan client deliverables and manage project budgets
• Act as programming lead for assigned studies or programs
• Set up study databases and e
  PRO/IRT (if applicable) based on provided specifications
• Write or review the Database Validation Plan and perform database validation/UAT in collaboration with CDM
• Review Data Validation Plans for feasibility and program edit checks in CDM systems and/or SAS
• Support CDM with data import/export and creation of data transfer specifications, liaising with vendors as needed
• Validate data transfer programming and manage user access rights
• Provide user support for EDC studies and execute database locks with CDM
• Escalate project issues or SOP deviations as required
• Contribute to system validation, including test script creation and UAT execution
• Participate in process development, SOP writing/review, and related training
• Provide input to proposals that include data management components and attend bid defense meetings as needed

Additional SAS Programming (if qualified)

• Perform SAS programming related to data management outputs (e. g. data listings, SAE reconciliation,
  - hoc reports)
• Develop and validate global SAS macros for data management processes
• Program/validate SDTM datasets, including define. XML and SDTM reviewer’s guides
• Provide training and mentoring related to SAS programming

Qualifications

• Bachelor’s degree, preferably in Life Science, Computer Science, or a related field
• Minimum of 8 years of relevant database programming experience in the pharmaceutical or CRO industry, including at least 5 years at a senior level
• Familiarity with CDMS systems and industry standards applicable for programming in a Gx
  P environment (e. g. 21 CFR Part 11, GAMP)
• Proven leadership skills and the ability to handle multiple tasks and meet deadlines
• Excellent verbal and written communication skills
• Strong ability to work effectively with sponsors and internal teams

What We Offer

We provide opportunities for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in patients’ lives.

Locations

Multiple locations in Europe - Hybrid or Remote