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

Responsibilities

Support study-level data management activities across oncology trials

Hands-on database build, CRF development, and edit check implementation

Execute data review plans and UAT for EDC and eCOA systems

Contribute to inspection readiness and study documentation

Collaborate with Biostatistics, Statistical Programming, and Clinical Operations

Experience Required

Degree in Life Sciences, Health Informatics, or a related discipline

CDM experience within pharma or biopharma; oncology experience required

Demonstrable experience working directly for a sponsor company

Working knowledge of EDC platforms (e.g., Rave, Oracle Clinical)

East Coast based only

Compensation DOE - $130,000 - $180,000 base salary + benefits