Clinical Research Coordinator

• 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. 
• 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, implements study-specific communications, and 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, attends study specific meetings as required or asked to do so, and reviews and responds to any monitoring findings and escalates issues.

• Bachelor's degree preferred, AS degree accepted with relevant clinical research experience
• Must have at least 1 year of CRC experience with recruitment, screening, and consents/enrollments of participants
• Computer skills with demonstrated abilities using web-based applications, electronic data capture, and MS Word or Excel
• Work independently in a fast-paced environment with minimal supervision at off-site facilities

Benefits
System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.