Director, Medical Safety
5.0
Töötajate arv: 20–50
Põhitegevusala: Teadus- ja arendustegevus loodus- ja tehnikateaduste vallas
Palk täpsustamata
Responsibilities
Medical review and oversight of clinical trial and post-marketing safety data, including adverse events, causality, and benefit-risk assessments, along with pharmacovigilance governance and leadership of medical safety teams.
Requirements
- Medical degree (MD)
- Medical licensure
- Pharmacovigilance
- Clinical research
- Good Clinical Practice (GCP)
- Safety reporting
- Medical monitoring
- People management
- Regulatory compliance
Employer offers
- Home-based work