Clinical Research Coordinator

Biopharma Informatic is seeking an experienced Clinical Research Coordinator (CRC) to join our team. This is an onsite position, open only to local candidates.We are looking for candidates with direct experience as a Lead CRC in clinical research trials conducted in physician or private practice settings. Please note that experience limited to hospital or university-based research roles does not fully align with this position.Key ResponsibilitiesLead the coordination and execution of clinical trials across all phases: start-up, enrollment, maintenance, and close-out.Ensure proper receipt, handling, and accountability of investigational product (IP).Conduct and document the informed consent process in compliance with protocols and regulations.Serve as a liaison between physicians, study sponsors, and Biopharma Informatic team members.Achieve or exceed study enrollment targets at assigned sites.Complete accurate and timely data entry into electronic data capture systems.Resolve data queries promptly to meet project timelines and support database lock.Maintain compliance with GCP, company SOPs, and industry regulations.QualificationsMinimum 2 -5 years of experience as a Lead Clinical Research Coordinator in a physician practice or private research setting.Strong understanding of investigational product (IP) receipt, handling, and accountability.Proven experience with the informed consent process.Demonstrated success in coordinating and managing clinical trials independently.Excellent organizational, communication, and problem-solving skills.Must be local to the area (onsite only; no relocation or remote work).