About Our Client
Internationally renowned pharmaceutical company in the Zug area, recruiting for a Pharmacovigilance Scientist.
Job Description
Key Responsibilities
* Manage processes for aggregate reports (PSURs, DSURs, PADERs, and local reports)
* Act as Subject Matter Expert (SME) on relevant safety requirements and company policies/procedures
* Support process improvement and implement/maintain processes
* Responsible for the Aggregate Reports Master Schedule and worldwide legislation overview
* Coordinate and author responses to safety questions from regulatory authorities
Requirements
* Master's degree in Life Sciences or related field
* 8+ years work experience in PV, including strong focus on authoring aggregate reports (minimum 2 years)
* Strong pharmacovigilance and drug development foundation, including knowledge of applicable clinical trial safety regulations and post-marketing safety regulations
* Ability to collaborate in a team and with external colleagues
* Familiarity with common data processing software and safety database systems
* Strong communication skills in English and organizational skills
About the Role
This is a 12 months contract with extension option. Opportunity to join a dynamic team and contribute to the discovery, development, and delivery of innovative therapies.