Provide medical management and expertise for clinical trials
Contribute medical expertise to study reports, regulatory documents, and manuscripts
Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials
Participate in new business development through involvement in proposal and sponsor meetings as requested
Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents
Follow specific research related protocol and lead others in strict adherence to the policies
Qualifications
Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred
Prior clinical tria...
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