Clinical Research Coordinator II
Nashville, Tennessee
Employer: System One Holdings, LLC
Industry:
Salary: Competitive
Job type: Full-Time
Position: Clinical Research Coordinator
Location: Nashville, TN- Onsite Role
Hours/Schedule: Monday-Friday/ 8-5
Type: Contract
Joule is currently looking for a Clinical Research Coordinator with a strong background in performing blood draws. This is a contract opportunity with the potential for extension. Primary responsibility is to screen, enroll and follow study subjects ensuring protocol compliance and monitoring while the subjects are on study. Responsible for all data collection, source documentation, completing study specific case report forms, and submission of adverse experience reports.
Duties and Responsibilities:
• 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
Location: Nashville, TN- Onsite Role
Hours/Schedule: Monday-Friday/ 8-5
Type: Contract
Joule is currently looking for a Clinical Research Coordinator with a strong background in performing blood draws. This is a contract opportunity with the potential for extension. Primary responsibility is to screen, enroll and follow study subjects ensuring protocol compliance and monitoring while the subjects are on study. Responsible for all data collection, source documentation, completing study specific case report forms, and submission of adverse experience reports.
Duties and Responsibilities:
• 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
Created: 2024-08-30
Reference: 324094
Country: United States
State: Tennessee
City: Nashville
ZIP: 37027
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