Lead Site Coordinator (South West Region)
Core
Lead a group of medical institutions in clinical trial conduct, acting as a liaison between the sponsor/CRO, site staff, and Principal Investigators to ensure protocol compliance and study success.
Role type
Senior Site/Study Coordinator (Lead)
Builds
Clinical trial operations and patient enrollment pipelines for medical institutions
Domain
Clinical Research / Healthcare
Deliverable
client delivery
Required skills
Clinical trial protocol management, patient recruitment and retention, data entry into EDC systems, regulatory document preparation, site quality checks, training and mentoring staff, contract and budget negotiation support, investigational product handling
Preferred skills
Master's degree in life science/pharmacy/nursing, ACRP/SOCRA certification, GCP certification, IATA certification, phlebotomy skills, experience with multi-therapeutic indications
Technologies
EDC/EMR vendor systems, Microsoft Office
Responsibilities
Supervise site-level staff on protocol-specific tasks, facilitate feasibility evaluations for new studies, assist in patient recruitment and eligibility confirmation, perform site quality checks for compliance, provide training to site staff on clinical research best practices, track patient enrollment targets, resolve data queries and adverse events, support contract negotiations and investigator payments, prepare for regulatory inspections and audits
Seniority
Senior, hands-on IC with mentorship responsibilities