Clinical Research Associate — I&I or Oncology; In-house
Listed on 2026-10-11
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Healthcare
Clinical Research, Oncology Care -
Research/Development
Clinical Research, Oncology Care
Role
Clinical Research Associate supporting Phase I-III oncology trials, focusing on site monitoring, study startup, data oversight, and regulatory compliance.
Responsibilitiesoversee CRO/vendor monitoring, ensure protocol adherence, perform site visits, SDV/SDR, manage regulatory documents, coordinate study startup activities, and collaborate with cross-functional teams.
RequirementsBachelor's in life sciences, nursing, pharmacy; 4+ years clinical monitoring experience including 1+ on-site; strong knowledge of ICH GCP, FDA regulations; hands-on with EDC, CTMS, eTMF (Medidata Rave preferred); valid driver’s license and passport; 30-40% travel.
High ValueOncology (solid tumor/hematology), Phase 1/2, RECIST 1.1, KPI dashboards, risk-based monitoring, sponsor oversight of CROs.
Work Setuphybrid with Boston office (70% presence), travel required.
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