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We provide pharmacovigilance services within clinical studies to our clients. Our team of experienced physicians logs, tracks, provides and reports SAEs and SUSARs to our clients and to the appropriate regulatory authorities and ethic committees in an expedited reporting procedure. The team is familiar with local safety reporting requirements in the different European countries and is always up-to-date.
The daily tasks of Safety Manager include:
- Receiving, processing, and archiving of serious adverse events (SAE) information
- Ensuring compliance with local and international requirements
- Expedited safety reporting
- Preparation of Period Safety Update Reports (PSURs) and Annual Safety Reports(ASRs)
- Data reconciliation of pharmacovigilance and clinical databases
We are looking for candidates with:
- University degree (or interns) in medicine
- Interest in clinical research
- Professional use of the English language; both written and oral
Experience in clinical research would be an advantage.
Scope International offers a friendly atmosphere in a highly motivated team, continuous professional training by knowledge sharing, space for individual competence and growth, stability. We offer full-time or part-time employment.
We'll inform just selected candidates.
Confidentiality is guaranteed.
An independent Full-Service CRO (Contract Research Organization) with 15 own offices in Europe and CRO partnerships in all other important clinical research regions offers a complete range of clinical development and consulting services to the pharmaceutical, biotechnology and medical device industries.
We have years of experience and expertise in research as well as a passion for science and providing quality solutions.
Scope International is expanding its services in Lithuania and is looking for a SAFETY MANAGER