Descrizione dell'offerta
Experteer Overview
In this role you will provide clinical, scientific, and strategic leadership for the planning, execution, and reporting of clinical trials. You act as Medpace's internal medical expert for study results interpretation and regulatory documents. You will participate in the development of new clinical projects, including study design and protocols. You will work across departments to ensure safety and compliance, and support business development through sponsor engagements. This hybrid, location‑flexible position offers the chance to shape therapeutic development at a leading CRO.
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 evaluations
- Participate in business development via proposals and sponsor meetings
- Coordinate with departments across feasibility, design, medical information, and document review/editing
- Ensure adherence to research protocols and policies
Responsabilità
- M.D. 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 package
- 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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