City of Hope
jobsnear.net
Regulatory Coordinator
Location:
United States
Category:
Clinical Trials Operations
Job Type:
Full-time
Pay Rate:
$34.64 – $53.70 per hour
As a Regulatory Coordinator at City of Hope, you’ll play a crucial role in assisting our investigators with the submission of human subject research to regulatory committees, contributing to the advancement of critical medical research. Reporting to the Portfolio Supervisors, Senior Director, Clinical Trial Office, and the CTO leadership team, you’ll facilitate prompt protocol submissions, serving as a liaison to external IRBs.
As a successful candidate, you will:
New Research Study Submission:
-
- Develop and maintain knowledge of institutional protocol submission procedures.
- Coordinate the preparation and submission of new studies to appropriate committees.
- Keep stakeholders informed of protocol approval and activation status.
Post Initial Approval Submissions:
-
- Prepare and submit amendments, continuing reviews, and deviations to appropriate committees.
- Participate in research audits and communicate status to the PI and research staff.
Regulatory Documents:
-
- Assist in maintaining Regulatory Binders for each study.
- Liaise with Protocol Coordinators, investigators, and sponsors.
- Attend meetings, conferences, and contribute to the training of new clinical trials staff.
Qualifications
Your qualifications should include:
- Bachelor’s degree.
- Two or more years of experience related to the management and conduct of clinical trials in an academic setting.
- Working knowledge of clinical trials, Federal, State, and Local Regulations, IRB requirements, consent form, and protocol development.
To help us track our recruitment effort, please indicate in your cover/motivation letter where (jobsnear.net) you saw this job posting.