Medical Trials Specialist
18 hours ago
Medpace is a leading full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
Key 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 protocol and lead others in strict adherence to the policies.
- M.D., specialization in Oncology, and current medical licensure;
- Board certification;
- Prior clinical trial research experience preferred;
- Previous experience in pharmaceutical-related clinical research is preferred.
- Flexible work environment;
- Competitive compensation and benefits package;
- Competitive PTO packages;
- Structured career paths with opportunities for professional growth;
- Company-sponsored employee appreciation events;
- Employee health and wellness initiatives.
$130,000 - $150,000 per year.
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