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We are seeking a highly experienced Clinical Research Director to join our dynamic team. The successful candidate will have overall responsibility for providing medical, scientific, and strategic leadership for the planning, execution, and reporting of clinical trials. This role acts as the internal medical expert and serves as a resource for the review, presentation, and interpretation of results in the Clinical Study Report.
The ideal candidate will have expertise in study design, protocol development, and project planning. They will also be involved in new business development through involvement in proposal and sponsor meetings as requested.
Responsibilities- 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 protocols and lead others in strict adherence to policies.
