Support the benefit–risk evaluation of Idorsia’s products and contribute to patient safety throughout the product lifecycle
Job Summary
Support the benefit–risk evaluation of Idorsia’s products and contribute to patient safety throughout the product lifecycle.
Lead signal management activities, contribute to the planning and preparation of periodic safety reports, and support the Drug Safety Physician in the analysis and review of safety data.
This role offers a great opportunity to develop your expertise while making a meaningful impact.
Matching Summary
Support the benefit–risk evaluation of Idorsia’s products and contribute to patient safety throughout the product lifecycle.
Skills & Requirements
Must-have
Signal management activities
Periodic safety reports preparation
Global pharmacovigilance regulations
MedDRA expert
Improvement initiative lead
Nice-to-have
Collaborative and science-driven environment
Eager to grow in drug safety
Curious and passionate about patient safety
Key Requirements
University degree in life science or equivalent
At least 10 years of experience in pharmacovigilance
At least 3 years of experience in writing regulatory safety documents
Solid knowledge of regulatory safety regulations and guidelines
Excellent communication, interpersonal and problem-solving skills
Strong organizational skills and project management skills
Effective communication in English
Excellent knowledge of MedDRA and WHO drug dictionary