Clinical Programmer

📌 Clinical Programmer –Remote | Global Pharma Project

We are looking for an experienced Clinical Programmer  to join a long-term, fully remote project within a leading international pharmaceutical environment. This role offers the opportunity to work on global clinical trials, contribute to regulatory submissions, and collaborate with cross-functional teams.

🔍 Position Overview:
The Clinical Programming  will lead programming activities across multiple studies, ensuring high-quality deliverables aligned with CDISC standards. The role includes defining data specifications, managing data flow, and supporting database lock processes.

💼 Responsibilities:

• Lead programming tasks for clinical trials, including SDTM mapping and validation
• Define CRF and external data specifications
• Perform and supervise data handling and UAT
• Develop and maintain SAS/SQL programs for reporting
• Ensure compliance with internal processes and regulatory standards
• Collaborate with CROs and internal stakeholders to ensure data integrity and timely delivery

🎓 Requirements:

• Bachelor’s/Master’s/PhD in Life Sciences, Statistics, or Information Technology
• Minimum 5 years of experience in clinical programming within pharma or CRO – mandatory
• Strong expertise in SAS programming and CDISC standards (SDTM, ADaM) – mandatory
• Familiarity with Pinnacle 21 and regulatory submission processes
• Excellent communication skills and ability to work independently in a global environment
• Fluent technical English