Job Summary
The Clinical Study Coordinator plays a crucial role in assisting healthcare facilities with the orchestration of clinical trial processes. This includes overseeing patient recruitment, ensuring adherence to study protocols, and managing data entry tasks. Serving as the central contact point among the sponsor, Contract Research Organization (CRO), and the medical site, this role is essential for facilitating effective study execution while maintaining regulatory standards.
Responsibilities
- Manage overall clinical trial activities with a focus on effective patient recruitment.
- Ensure compliance with study protocols and regulatory requirements.
- Coordinate communication between the sponsor, CRO, and medical site.
- Oversee data entry and maintenance of study records.
Qualifications
- Minimum of two years of experience in coordinating clinical research involving human participants.
- Certifications required include GCP (Good Clinical Practice), IATA (International Air Transport Association), CPR (Cardiopulmonary Resuscitation), and phlebotomy.
- Possession of a professional clinical research certification is desirable.
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.
