Descrizione dell'offerta
Experteer Overview
In this role you will provide medical, scientific and strategic leadership for planning, executing, and reporting clinical trials. You will serve as Medpace’s internal medical expert and support review and interpretation of results in study reports. You will contribute to the development of new clinical projects, including study design and protocols, across a dynamic, hybrid work environment. You will collaborate with cross-functional teams to advance therapeutic development and ensure rigorous safety and regulatory standards.
Retribuzione / Benefits
- Provide medical management and expertise for clinical trials
- Contribute medical input to study reports, regulatory documents and manuscripts
- Manage safety issues in trials and collaborate on evaluation
- Participate in new business development through proposals and sponsor meetings
- Coordinate with other departments across feasibility, design, education, medical information management and editing of medical documents
- Ensure adherence to research protocols and lead others in compliance
Responsabilità
- MD degree or equivalent
- Board certification and current medical licensure preferred
- Prior clinical trial research experience preferred
- Previous experience in pharmaceutical-related clinical research preferred
Requisiti fondamentali
- Flexible work environment
- Competitive compensation and benefits
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Candidatura e Ritorno (in fondo)
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