Clinical Research Coordinator
4 weeks ago
Culmen International is seeking a skilled Clinical Protocol Developer to join our team in Portsmouth, VA. As a key member of our research team, you will assist physicians and scientists in developing, writing, and producing human and animal research protocols in support of military medicine research programs.
Key Responsibilities:
- Assist with the preparation of investigator-initiated trials, including coordination of protocol submission, submission of amendments, and regulatory compliance reports.
- Contribute to the preparation and modification of internal study budgets.
- Ensure PI-initiated protocols contain quality research design and meet DOD standards for ethics and compliance.
- Assist with addressing Scientific Review Committee (SRC), Institutional Review Board (IRB), and other committee queries.
- Attend and assist with the planning of committee meetings for disease-specific working groups to facilitate research development.
Requirements:
- Bachelor's Degree
- Minimum five (5) years of Clinical Research experience
- Ability to obtain Public Trust/NACI clearance
About Culmen International:
Culmen International is committed to enhancing international safety and security, strengthening homeland defense, improving global health and humanitarian programs, and optimizing government operations. With experience in over 140 countries, we help our customers to accomplish critical missions in challenging environments worldwide.
Benefits:
- Exceptional Medical/Dental/Vision coverage with 100% of the premiums paid by the company for all employees and their eligible dependents for full-time positions (including same or opposite-sex domestic partners)
- 401k - Vested immediately and 4% match
- Life insurance and disability paid by the company
- AFLAC Available
- Tuition Assistance
- 12 Paid Holidays
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