Data Management Consultant

Clin Ops Data Consultant (Oncology) – Contract Role - East CoastContract Length: Initial 6 months (strong extension potential through 2029) Location: Remote (Preference East Coast) Hours: ~20 hours/week (likely to increase) Start Date: Late May (firm requirement)OverviewA biotech organisation is seeking a hands-on Clin Ops Data Consultant to support an upcoming Phase 1 oncology trial. This is a critical hire needed to establish the study database ahead of first patient enrollment (planned for Sept/Oct).This role is execution-focused and suited to someone who can operate with minimal oversight, take ownership, and work effectively in a lean, fast-paced environment.Key ResponsibilitiesBuild and configure the clinical study database to support both clinical and translational endpointsIntegrate and manage data flows from external vendorsCollaborate closely with a CRO operating across time zonesEnsure readiness of data systems ahead of study start and patient enrollmentSupport ongoing data management activities as the study progressesRequired ExperienceStrong background in Clinical Data Management / Clin Ops Data rolesProven experience in oncology clinical trials (essential)Experience supporting Phase 1 (early-phase) studiesAbility to work independently and proactively with minimal directionHands-on, execution-focused mindset (not purely strategic)Preferred ProfileExperience in small to mid-size biotech environments (highly valued)Demonstrated “roll up your sleeves” approachComfortable working with external vendors and CROs globallyADC experience not requiredAdditional ContextThis is an urgent hire, with onboarding required by late MayLong-term potential to remain involved through:Phase 1 enrollment (2027)Expansion phase (2028)Database lock (2029)