Clin Ops Data Consultant (Oncology) Contract Role - East Coast Contract 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) Overview A 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 Responsibilities Build and configure the clinical study database to support both clinical and translational endpoints Integrate and manage data flows from external vendors Collaborate closely with a CRO operating across time zones Ensure readiness of data systems ahead of study start and patient enrollment Support ongoing data management activities as the study progresses Required Experience Strong background in Clinical Data Management / Clin Ops Data roles Proven experience in oncology clinical trials ( essential ) Experience supporting Phase 1 (early-phase) studies Ability to work independently and proactively with minimal direction Hands-on, execution-focused mindset (not purely strategic) Preferred Profile Experience in small to mid-size biotech environments (highly valued) Demonstrated roll up your sleeves approach Comfortable working with external vendors and CROs globally ADC experience not required Additional Context This is an urgent hire , with onboarding required by late May Long-term potential to remain involved through: Phase 1 enrollment (2027) Expansion phase (2028) Database lock (2029)