You will be responsible for pharmacovigilance of products in development and undergoing clinical trials, as well as signal management for authorized products
Job Summary
You will be responsible for pharmacovigilance of products in development and undergoing clinical trials, as well as signal management for authorized products.
Your role involves ensuring the interface between the Vigilance Department and R&D, monitoring product safety profiles throughout their lifecycle, and contributing to regulatory submissions.
Pierre Fabre offers an attractive compensation and benefits package including profit-sharing, employee stock ownership with matching, health and welfare coverage, and additional paid time off.
Matching Summary
You will be responsible for pharmacovigilance of products in development and undergoing clinical trials, as well as signal management for authorized products.
Skills & Requirements
Must-have
Pharmacovigilance of products in development
Signal detection and analysis
Risk management activities
Regulatory compliance
Medical expertise in signal detection
Nice-to-have
Pioneering company in expansion
Commitment to diversity and inclusion
Engaged in corporate social responsibility
Key Requirements
Physician or Pharmacist
Minimum 5 years experience in pharmaceutical vigilance
Experience in clinical trial vigilance for medicinal products