What are the responsibilities and job description for the Clinical Research Coordinator position at System One?
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:
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:
- 1 years of CRC experience supporting intervention drug studies
- Proficient performing phlebotomy and processing/shipping samples
- Excellent communication skills and ability to work collaboratively
- Ability to work independently in a fast-paced, high volume environment with minimal supervision
- Organizational and prioritizing capabilities
- Computer skills with demonstrated abilities using web-based applications, electronic data capture, and MS Word or Excel
- Professional communication
- Communicate and work effectively with a diverse team of professional
- Interpersonal skills, detail-oriented and meticulous
- Work independently in a fast pace environment with minimal supervision at off-site facilities
