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 IT Asset Administrator will oversee procurement and management of IT assets while ensuring compliance and accurate record-keeping.
Join PrimeVigilance as a Senior Pharmacovigilance Officer, managing case processing and contributing to patient safety.
The ITSM Engineer will manage and optimize IT service management processes and tools to enhance service delivery and user experience.
Join PrimeVigilance as a Senior PV Officer to manage ICSR activities and support pharmacovigilance processes.
Join Ergomed Group as a Legal Counsel, providing legal guidance and managing contracts in the pharmaceutical and CRO industry.
Join Ergomed as a Senior Statistical Programmer to contribute to clinical studies through SAS programming and data management.
PrimeVigilance is looking for a Senior Pharmacovigilance Officer to manage case processing and mentor junior staff in a supportive, global environment.
Join PrimeVigilance as a Senior Pharmacovigilance Officer to manage case processing services and contribute to patient safety.
Join PrimeVigilance as a Junior PV Officer to manage case processing services in a supportive and diverse environment.
Ergomed Group is seeking a Director of Business Development to lead strategic sales initiatives in the Southeast USA.
Join PrimeVigilance as a Freelance Consultant for Local Literature Screening, requiring fluency in German and expertise in pharmacovigilance.
Join PrimeVigilance as a Freelance Consultant for Pharmacovigilance and Regulatory Affairs, working 0.5 FTE in a dynamic international team.
Join PrimeVigilance as a Freelance Consultant for Pharmacovigilance and Regulatory Affairs, working 0.5 FTE in a dynamic international team.
The Pharmacovigilance Project Manager will lead and manage long-term client engagements in the pharmacovigilance sector.
The Director of Quality Management & Compliance will lead the QA team, oversee quality management activities, and ensure compliance with regulatory standards.