Clinical Research Regulatory Administrator responsible for administrative and regulatory support, including maintaining documentation, ensuring compliance, and supporting IRB submissions.
Requirements
- Bachelor’s degree in life sciences, health sciences, public health, business administration, or a related field
- 0-2 years of relevant experience in healthcare administration, clinical research, regulatory coordination, or a related environment
- Strong attention to detail and ability to maintain accurate documentation
- Excellent organizational and time-management skills
- Clear written and verbal communication skills
- Comfort with learning new systems and software platforms
- Proficiency with Microsoft Office
Benefits
- Generous Paid Time Off
- 401k Matching
- Retirement Plan
- Tuition Reimbursement
