Clinical Data Management Programmer III

Join a dynamic and growing clinical research organisation at the forefront of data-driven innovation in clinical trials. We are committed to delivering high-quality, reliable data solutions that accelerate drug development and improve patient outcomes worldwide. Our collaborative, fast-paced environment empowers talented professionals to make a meaningful impact while continuously developing their skills.

This is an exciting opportunity for a detail-oriented and technically strong CDM professional to expand their expertise, contribute to process improvements, and work with industry-leading tools in a highly collaborative environment.

What You’ll Do

Technical Programming & Study Delivery

• Lead and support technical and programming activities for allocated Clinical Data Management projects.
• Review programming requirements and timelines in collaboration with the Manager - CDM Programming and the Lead CDM.
• Ensure programming deliverables are completed to agreed timelines and quality standards.
• Support programming activities required for study reporting and data deliverables.
• Be aware of and work to the standards appropriate to the study.

Quality, Compliance & Governance

• Perform code reviews to ensure programming quality, consistency, and compliance with company standards.
• Conduct internal audits and reviews of study documentation, programming outputs, and p