The Clinical Study Coordinator supports medical institutions by managing clinical trial activities, including patient recruitment, protocol adherence, and data entry. They act as the primary liaison between the sponsor, CRO, and the medical site to ensure study delivery and regulatory compliance. Candidates must have at least two years of experience coordinating clinical research studies involving human subjects. Required certifications include GCP, IATA, CPR, and phlebotomy, with professional clinical research certification preferred.
PSI CRO provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
