About this role
Clinical Protocol Developer at Culmen International, LLC. Location: Portsmouth, Virginia, United States. Role: developing protocols, preparing submissions, conducting reviews Requirements: Bachelor's degree, 5 years clinical research experience, ability to obtain Secret clearance; experience developing/writing research protocols, eIRB and clinicaltrials.gov submissions, literature reviews, and study documentation. Category: Research and Development (R&D) Seniority: Senior Level Tools: eIRB, clinicaltrials.gov Commitment: Full Time Workplace: Onsite Languages: English