* International pharmaceutical company
* 12-month contract with extension option
About Our Client
An internationally renowned pharmaceutical company in the Zug area is recruiting a Pharmacovigilance Scientist.
Job Description
Key Responsibilities
* Manage processes for aggregate reports, including PSURs, DSURs, PADERs, and local reports.
* Act as Subject Matter Expert (SME) on relevant safety requirements and company policies/procedures related to pharmacovigilance activities and aggregate reports.
* Support process improvement, implementing and maintaining processes.
* Responsible for the Aggregate Reports Master Schedule and worldwide legislation overview.
* Coordinate and author responses to safety questions from regulatory authorities.
The Successful Applicant
* Masters degree or equivalent in Life Sciences or related field.
* 8+ years work experience in PV, including strong focus on authoring aggregate reports.
* Strong pharmacovigilance and drug development foundation, including knowledge of applicable clinical trial safety regulations and post-marketing safety regulations.
* Able to collaborate in a team, cross-functionally, and with external colleagues.
* Familiarity with case processing, expedited reporting rules, and safety database concepts.
* Knowledge of common data processing software and common safety database systems.
* Strong communication skills in English and organizational skills.
What's on Offer
Part of a dynamic team contributing to the discovery, development, and delivery of innovative therapies to improve patients' lives.