Overview
In this role you will provide medical leadership for hepatology-focused clinical trials, acting as the internal medical expert and overseeing study design, reports, and safety reviews. You will collaborate across departments to ensure compliant trial execution and contribute to new clinical projects. The position supports a hybrid work model and involves liaising with sponsors and regulators to advance therapeutic development. This role offers meaningful impact through shaping trial strategy and interpretation of results within a global CRO environment.
Arbeidsvoorwaarden / Benefits- 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
Verantwoordelijkheden- Provide medical management and expertise for clinical trials
- Contribute medical input to study reports, regulatory documents, and manuscripts
- Manage safety issues in trials and assess adverse events
- Participate in new business development through proposals and sponsor meetings
- Coordinate with multiple departments across all study phases including feasibility, design, and medical information management
- Lead adherence to research protocols and policies
Belangrijkste vereisten- MD degree or equivalent (required)
- Board certification and current medical licensure preferred
- Prior clinical trial research experience preferred
- Previous experience in pharmaceutical-related clinical research preferred
Solliciteren