Job Summary
The Director of Pharmacovigilance is responsible for guiding the pharmacovigilance team, managing all safety-related functions for products throughout their lifecycle, from clinical development to post-marketing phases. This role is vital in ensuring patient safety and regulatory compliance.
Responsibilities
- Oversee signal detection and medical safety monitoring during clinical trials.
- Ensure adherence to both national and international safety regulations.
- Lead the pharmacovigilance team in safety-related activities and product assessments.
- Facilitate safety reporting and manage regulatory submissions effectively.
Qualifications
- Doctorate Degree (MD) is essential.
- Minimum of 10 years’ experience in clinical safety.
- In-depth knowledge of the product lifecycle and safety reporting processes.
- Familiarity with regulatory requirements regarding pharmacovigilance.
