Clinical Research Regulatory Coordinator Cancer Center Protocol Office-(3302823)
Description
GENERAL SUMMARY / OVERVIEW STATEMENT :
The Cancer Center Protocol Office is seeking motivated, detail-oriented individuals to join our team as a Clinical Research Regulatory Coordinator.
The Cancer Center Protocol Office is a centralized research office that supports clinical researchers in all disciplines within the Cancer Center.
Our office promotes and facilitates clinical research by providing comprehensive services to physicians conducting clinical trials while ensuring compliance with all regulatory requirements.
The Clinical Research Regulatory Coordinator I (CRRCI) works under general supervision to ensure the regulatory requirements for clinical trials are met.
This position involves working with clinical teams, Institutional Review Boards (IRB), clinical trial sponsors and federal regulatory agencies.
The CRRCI will be trained on the institutional and federal regulations governing clinical research. This position does not involve patient contact.
PRINCIPAL DUTIES AND RESPONSIBILITIES :
The following regulatory duties will be performed under general supervision by the Clinical Research Manager :
- Maintain and organize study specific regulatory binders
- Prepare and submit protocol amendments, continuing reviews, and safety reports to the IRB
- Revise informed consent documents to include new risk information and / or updated protocol requirements through the course of the study
- Manage adverse event and deviation / violation / exception documentation for all enrolled patients and report to the sponsor and IRB as required
- Submit Data and Safety Monitoring Reports
- Maintain source documentation of correspondence with the IRB, investigators, and sponsors throughout the clinical trial process
- Collect, complete, and submit essential regulatory documents to various regulatory entities
- Participate in monitoring visits and file all monitoring visit correspondence
- Ensure appropriate documentation of delegation and training for all study staff members
- Maintain screening and enrollment logs
SKILLS / ABILITIES / COMPETENCIES REQUIRED :
- Careful attention to detail
- Good organizational skills
- Ability to follow directions
- Good communication skills
- Computer literacy
- Working knowledge of clinical research protocols
Qualifications
EDUCATION :
- BA / BS degree required EXPERIENCE :
- None
- None
SUPERVISORY RESPONSIBILITY :
None
WORKING CONDITIONS :
- Duties may be performed in a combination of on-site and / or remote work setting.
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