Medix
The Clinical Research Coordinator (CRC) is responsible for coordinating and managing clinical research studies under the supervision of a Principal Investigator (PI). This role ensures that studies are conducted according to the study protocol, regulatory requirements, and institutional policies while maintaining participant safety and data integrity.
Key Responsibilities
Coordinate all aspects of assigned clinical trials, including participant recruitment, screening, enrollment, and follow-up.
Obtain informed consent from study participants.
Collect, record, and maintain accurate study data and documentation.
Schedule and conduct study visits and procedures according to protocol.
Communicate with sponsors, monitors, and regulatory bodies as needed.
Prepare and submit regulatory documents, including IRB submissions and study updates.
Maintain inventory of study supplies and manage investigational products (if applicable).
Ensure compliance with Good Clinical Practice (GCP) and institutional standards.
#J-18808-Ljbffr
Key Responsibilities
Coordinate all aspects of assigned clinical trials, including participant recruitment, screening, enrollment, and follow-up.
Obtain informed consent from study participants.
Collect, record, and maintain accurate study data and documentation.
Schedule and conduct study visits and procedures according to protocol.
Communicate with sponsors, monitors, and regulatory bodies as needed.
Prepare and submit regulatory documents, including IRB submissions and study updates.
Maintain inventory of study supplies and manage investigational products (if applicable).
Ensure compliance with Good Clinical Practice (GCP) and institutional standards.
#J-18808-Ljbffr