Ergomed is a specialized mid-size pharmacovigilance service provider, established in 2008, and is part of the Ergomed group. With a commitment to global organic growth, Ergomed has built a strong presence across Europe, North America, and Asia, offering services in Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance. The company prides itself on maintaining long-lasting relationships with pharmaceutical and biotechnology partners, covering all therapy areas, including medical devices. Ergomed values its employees by investing in their training and development, promoting well-being and mental health, and fostering a healthy work-life balance to ensure high-quality client service.
The Project Management Assistant will provide administrative support to the project management team, ensuring efficient operations and effective communication.
The PV Physician II is responsible for the medical review of safety reports and literature, contributing to pharmacovigilance efforts.
The Senior PV Physician I role involves reviewing safety reports and supporting pharmacovigilance efforts in a global environment.
Join PrimeVigilance as a PV Physician II, responsible for reviewing safety reports and supporting pharmacovigilance activities.
The Project Finance Analyst will manage financial aspects of projects, ensuring accurate forecasting and reporting.
Join Ergomed Group as a Contract Project Manager focusing on global clinical trials in Radiopharmaceuticals and various cancers.
Join PrimeVigilance as a Local Contact Person for Pharmacovigilance and Regulatory Affairs, ensuring compliance with local regulations.
The PSMF Associate manages the creation and maintenance of Pharmacovigilance System Master Files in compliance with global regulations.
The Local Contact Person for Pharmacovigilance and Regulatory Affairs ensures compliance with local regulatory requirements while supporting pharmaceutical partners.
Join Ergomed as a Senior Statistical Programmer to lead statistical programming efforts in clinical studies.
Join PrimeVigilance as a Specialist in Regulatory and Pharmacovigilance, driving compliance and project management in a global context.
The Manager, Regulatory & Pharmacovigilance Network will lead regulatory projects and ensure compliance while mentoring junior staff.
Join PrimeVigilance as a Safety Reporting Manager, Team Leader to oversee safety reporting staff and ensure compliance in pharmacovigilance.
Join PrimeVigilance as a Medical Information Associate to support medical inquiries in English and French.