The Clinical Research Coordinator II handles administrative activities generally associated with the conduct of clinical trials.
Requirements
- Manages research project databases
- Develops flow sheets and other study related documents
- Completes source documents/case report forms
- Provides guidance to less experienced staff
- Interfaces with research participants
- Determines eligibility and consents study participants according to protocol
- Approves orders for supplies and equipment maintenance
- Assists in developing recruitment strategies and conducting screenings for study participants
- Supervises collection of study specimens and processing
- Establishes case packages for study procedures
- Monitors scheduling of procedures and charges
- Coordinates other services as needed
- Ensures compliance with research protocols
- Reviews case report forms and audits for accuracy with source documents
- Attends monitoring meetings with sponsors
- Prepares regulatory submissions
- May perform phlebotomy or diagnostics with appropriate credentialing and training
- Performs related approved responsibilities as required
Benefits
- Emory University is an equal opportunity employer
- Emory University complies with Section 503 of the Rehabilitation Act of 1973
- Emory University complies with the Vietnam Era Veteran's Readjustment Assistance Act