
1001 - 5000 employees
Founded 1997
đź Consulting
đĽ Healthcare
đŚ Logistics
Consulting ⢠Healthcare ⢠Logistics
ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.
đ August 4
Where this job comes from
Posted on ERGOMED's careers page, not through a job board
First seen by Remote Rocketship August 4
Still open on ERGOMED's site. Checked 5 hours ago.

1001 - 5000 employees
Founded 1997
đź Consulting
đĽ Healthcare
đŚ Logistics
Consulting ⢠Healthcare ⢠Logistics
ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.
⢠Act as the primary contact point for project-related matters ⢠Manage client expectations and ensure client satisfaction with PrimeVigilance services ⢠Ensure delivered work meets or exceeds client expectations ⢠Prepare project scope and objectives based on signed client agreements ⢠Plan project activities, deadlines, and interim milestones ⢠Prepare reports for clients and PrimeVigilance management, including monthly reports used as a basis for invoicing
⢠Proven track record in pharmacovigilance activities, including processing and quality review of ICSRs ⢠Experience writing or contributing to aggregate reports ⢠Experience with literature screening and reconciliation ⢠Experience preparing SOPs ⢠Pharmacovigilance project management experience, ideally from a service provider or CRO ⢠Health Care Professional or Life Science Graduate ⢠Comfortable communicating at senior levels within pharmaceutical organizations ⢠Good leadership qualities ⢠Skills in planning, mentoring, meeting facilitation, communication, and problem solving
⢠Remote work option ⢠Flexible work environment ⢠Growth opportunities ⢠Collaborative and supportive team culture ⢠Global work environment ⢠Belonging and inclusive workplace ⢠Opportunity to contribute to patient safety and pharmaceutical treatment outcomes
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