Job Description: Clinical Research Study Coordinator
We are seeking a motivated and organized Clinical Research Study Coordinator to oversee the day-to-day operations of clinical trials at our research site. The Study Coordinator will ensure studies are conducted efficiently, ethically, and in compliance with protocols, regulatory requirements, and company standards.
Key Responsibilities:
- Coordinate and manage all aspects of clinical trials, including participant recruitment, enrollment, and retention.
- Schedule and conduct study visits, collect data, and ensure accurate documentation in case report forms (CRFs) and source documents.
- Maintain regulatory and study-related documents, including informed consent forms and IRB submissions.
- Ensure compliance with study protocols, Good Clinical Practice (GCP), and applicable regulations.
- Monitor participant safety and report adverse events to the Principal Investigator (PI) and sponsors.
- Collaborate with study sponsors, monitors, and site staff to ensure successful trial execution.
- Maintain inventory of study supplies, including investigational products and lab kits.
Qualifications:
- Bachelor’s degree in a healthcare-related field or equivalent experience (nursing, life sciences, etc.).
- Prior experience in clinical research preferred.
- Knowledge of GCP, FDA regulations, and clinical trial processes.
- Strong organizational, communication, and interpersonal skills.
- Proficiency in data entry and familiarity with clinical trial management systems (CTMS) is a plus.
Join our team and be part of advancing medical research while providing exceptional care to study participants!
