Medical Trials Director
1 week ago
Job Title: Medical Trials Director
About the Role:
We are seeking a highly skilled Medical Trials Director to join our team at Medpace. As a key member of our organization, you will be responsible for leading clinical trials from initiation to close-out, ensuring compliance with regulatory requirements and good clinical practice guidelines.
The successful candidate will have overall responsibility for ensuring that all clinical trials are conducted safely and efficiently, and that high-quality data is collected and reported. This will include contributing medical expertise to study reports, regulatory documents, and manuscripts, as well as managing safety issues in clinical trials.
Responsibilities:
- Lead clinical trials from initiation to close-out, ensuring compliance with regulatory requirements and good clinical practice guidelines;
- 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.
Requirements:
- M.D. with board certification and current medical licensure;
- Prior clinical trial research experience; and
- Previous experience in pharmaceutical-related clinical research is preferred.
Compensation and Benefits:
This role offers a competitive compensation package, including a salary of approximately $260,000 per annum, plus benefits such as flexible work environment, competitive PTO packages, and structured career paths with opportunities for professional growth.
About Medpace:
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach.
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