Clinical Research Coordinator

Clinical Research Coordinator at MCKESSON

• enroll patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up of eligible participants according to protocol requirements
• review study design and inclusion/exclusion criteria with physician and patient
• ensure the protection of study patients by verifying informed consent procedures and adhering to protocol requirements
• collect, complete, and enter data into study specific case report forms or electronic data capture systems within study required timelines
• ensure the integrity of the data submitted on case report forms or other data collection tools by careful source document review and monitoring data for missing or implausible data
• create study specific tools for source documentation when not provided by sponsor
• generate and track drug shipments, lab kits, and other supplies
• accurately and completely document protocol requirements according to site work instructions and standard operating procedures (SOPs)
• track and report adverse events, serious adverse events, protocol waivers, and deviations
• maintain accurate and complete records, including regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, screening and enrollment logs, and study communications
• coordinate regular site research meetings
• attend study-specific on-site meetings/visits, investigator meetings, conference calls, and other coordinator meetings, as required
• work closely with monitors, study teams, and site staff to ensure quality study data
• communicate site status through a weekly activity report to appropriate site/management colleagues

• Knowledge of medical and research terminology
• Knowledge of FDA Code of Federal Regulations and GCP
• Knowledge of the clinical research processes
• Public presentation skills
• The ability to manage multiple ongoing priorities and projects with a diverse team of professionals

• 401k matching
• Health insurance
• Flight privileges

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials.