Pv Associate

PV Associate (m/w/d)
- Your tasks

The PV Associate supports the responsible PV Manager in their responsibilities, including but not limited to
- Documenting, processing and reporting adverse drug reactions received from all sources (post-marketing and clinical trials), including scientific literature
- Compilation of periodic aggregate reports (PBRERs/DSURs)
- Periodic reconciliation with business partners and affiliates as well as internal reconcilications (complaints/medical inquiries)
- Contribute to the compilation and management of Standard Operation Procedures (SOP)
- Participate in and support the conduct of inspections
- Your duties
- University degree in pharmacy, biology or other Life Science
- First working experience in pharmacovigilance would be an advantage
- Highly structured and analytical way of work
- Strong team player with the motivation to work cross-functionally
- Ability to cope with high workload and to work under time pressure
- Excellent communication skills, including proficiency in written and spoken English
- Your benefits
- Personal initiative and taking responsibility for tasks and projects
- Lively exchange, curiosity and enthusiasm for creative and innovative ideas
- Diverse learning culture and individual development opportunities
- Respectful and open cooperation in a committed team
- International and growing family business with short decision-making processes, financial independence and long-term action
- New Work, flexible working hours and mobile working
- A wide range of benefits (free drinks, health and sports offers, canteen, JobRad)
- Onboarding and mentoring programme