Job Description
📋 Description Serve as day-to-day contact for CROs and vendors; track deliverables and timelines. Review CRO-provided study documents for completeness and quality. Coordinate startup activities such as site activation and regulatory document collection. Maintain trackers, timelines, and action logs; enable cross-functional visibility. Attend study team meetings; document minutes and follow up on actions. Track protocol deviations and coordinate resolution with CROs and teams. 🎯 Requirements Bachelor’s degree required; scientific/health field preferred. 6+ years in clinical operations or clinical research; sponsor-side a plus. Foundational understanding of GCP, ICH guidelines, and trial processes. Experience working with CROs or clinical vendors in coordination. Familiarity with CTMS, EDC, and eTMF platforms. Ability to travel up to 20% domestically and internationally. 🎁 Benefits Annual bonus opportunity. Equity compensation. Competitive benefits package.
