
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.
đĽ 7 minutes ago
đ§đŚ Bosnia and Herzegovina â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ§Ş Clinical Research
đť Ghost score 18%
Where this job comes from
Posted on ERGOMED's careers page, not through a job board
First seen by Remote Rocketship 7 minutes 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.
⢠Perform on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visits ⢠Ensure investigational site facilities and staff remain adequate for study conduct ⢠Identify investigators and verify their qualifications, resources, facilities, equipment, and staff throughout the study ⢠Train investigational site staff as necessary ⢠Support preparation of regulatory and/or EC submissions when applicable ⢠Participate in mentoring and training new staff ⢠Perform co-monitoring visits to assess junior staff performance
⢠College/University degree in Life Sciences or an equivalent combination of education, training & experience ⢠Extensive on-site monitoring experience in Phase 2/3 trials ⢠Ideally, experience with complex trials in oncology or rare disease ⢠Full working proficiency in English ⢠Ability to plan, multitask and work in a dynamic team environment ⢠Communication, collaboration, and problem-solving skills ⢠Ability to travel ⢠Full driving license required
⢠Remote work option ⢠Work-life balance ⢠Career growth opportunities ⢠Collaborative international team environment ⢠Mentoring and training opportunities ⢠Opportunity to make a difference by helping bring safe and effective pharmaceutical treatments to patients ⢠Diverse and inclusive workplace where every voice counts
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đ October 2
Clinical Research Associate conducting onsite monitoring and regulatory support for PSI, a contract research organization. Managing clinical-trial sites across Bosnia and Herzegovina.
đ September 29
Clinical Research Associate monitoring clinical trials for PSI, a contract research organization. Conducting site visits, supporting study startup, regulatory submissions, audits, and inspections.