Job Summary
A non-profit healthcare organization is filling a position for a Telecommute Regulatory Affairs Oncology Research Specialist in Charlotte.
Candidates will be responsible for the following:
- Assisting with regulatory documentation associated with oncology research projects/clinical trials
- Participating in the research start-up activity
- Maintaining all assigned study regulatory obligations are managed compliantly
Applicants must meet the following qualifications:
- Mobile within the entire healthcare system and other locations that participate in clinical trials
- Must speak and read/write clearly in English
- Ability to assist in maintenance of filing systems, including records management and data repositories
- Requires corrected vision and hearing within normal range
- Ability to assist in the monitoring of clinical trial compliance by reporting issues and problems appropriately