A well-established, secure and commercially active biopharma is expanding its US clinical data management team. This is a hands-on lead CDM role within a fully in-house function.

Responsibilities

• Lead study-level data management activities across assigned oncology trials
• Hands-on database build, CRF design, edit check development, and data transfer specifications
• Own data review plans, UAT for EDC and eCOA systems, and audit trail activities
• Support regulatory submissions and contribute to inspection readiness
• Collaborate cross-functionally with Biostatistics, Statistical Programming, and Clinical Operations

Experience Required

• Degree in Life Sciences, Health Informatics, or a related discipline
• Substantial CDM experience within pharma or biopharma
• Oncology experience required
• Demonstrable experience working directly for a sponsor company
• Hands-on expertise with EDC platforms (e.g., Rave, Oracle Clinical)
• East Coast based only

Compensation DOE - $170,000 - $210,000 base salary + benefits