Job Summary
A healthcare company is seeking a Telecommute Regulatory Affairs Oncology Research Coordinator in Charlotte.
Individual must be able to fulfill the following responsibilities:
- Coordinating regulatory document submissions for clinical trial start-up
- Assisting in the development, improvement and review of Standard Operating Procedures and processes
- Participating in sponsor study start-up and follow-up meetings as appropriate
Qualifications for this position include:
- Minimum of 3 years clinical research experience with a pharmaceutical company or CRO or equivalent experience
- Ability to coordinate and prepare for internal and external audits
- Ability to review documents and processes for quality assurance
- Ability to collaborate on billing and financial activity with Research Finance
- Ability to ensure timely and accurate submission of data
- Ability to provide educational and technical assistance to research staff
