Job Description

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

Requirements

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.

Company offers

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.

Additional information

We'll inform just selected candidates.
Confidentiality is guaranteed.