What are the responsibilities and job description for the Clinical Research Coordinator position at System One Holdings, LLC?
Title : Clinical Research Coordinator
Location : Nashville, TN
Type / Duration : Contract, 6 months, highly renewable
Duties and Responsibilities :
Duties include but are not limited to :
- Supports enrolling patients onto the clinical trial through screening, enrollment and follow up of eligible subjects according to protocol requirements
- Ensures the protection of study patients by verifying informed consent procedures and adheres to protocol requirements / compliance
- Collects, completes, and enters data into study specific case report forms or electronic data capture systems
- Ensures timely and accurate data completion
- Collects blood samples and tracks shipments and requests supplies as needed
- Implements study-specific communications
- Ensures timely adherence to protocol requirements
- Responsible for completion of all required documentation
- Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, subject logs and study-related communications
- Communicates all study-related issues to appropriate study colleagues or manager
- Apprises principal investigator and management of all study specific medical issues for guidance
- Attends study specific meetings as required or asked to do so
- Reviews and responds to any monitoring findings and escalates issues
Requirements :