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| Department: | Nursing _ MS |
| Location: | Savannah, GA |
Gastroenterology Consultants of Savannah
Position is in person - onsite at main clinic located at:
519 Stephenson Ave, Savannah GA 31405
Job Description
The Clinical Research Coordinator (CRC) is responsible for managing clinical trial performance, including study participant enrollment, study-specific documentation, and study-related training, at a GI group located in Birmingham, Alabama, with two to three close proximity satellite offices.
Primary Responsibilities
· Coordinate a clinical trial (e.g., blood draw/biomarker study) conducted by a supervising PI in accordance with FDA, GCP and protocol guidelines, including:
· screening participants
· obtaining informed consent
· coordinating visits and procedures
· managing lab kits
· collecting and documenting data ( study records, including regulatory forms, drug accountability records, and progress reports)
· reporting any adverse events
· Identify study-related issues, potential problems, or inconsistencies, and take action as appropriate.
· Review all study protocols and train applicable personnel at each assigned site.
· Communicate study, or protocol, issues to the CRO and/or Sponsor, Site Lead, Manager, Principal or Sub-Investigator and other members of the study team, as applicable.
· Ensure data collected for the study is accurate, attributable, and contemporaneous
· Maintain timely EDC data entry and query resolution.
· Complete all queries in a timely manner
· Attend conference calls for the company or Sponsor as needed
· Perform other study-related duties as assigned.
· Ensure that the company and the sites are adhering to all applicable federal and/or local regulatory standards.
Requirements:
A team player who is detail-oriented