Job Overview
Job description
- Location:
- Germany
- Work arrangement:
- On-site
Role Summary
Join our global team as a Pharmacovigilance Specialist
Pharmacovigilance Specialist is responsible for assuring compliance with local and regional Quality Management System and interact, exchange relevant safety and pharmacovigilance information.
Position is remote/home-based in Germany.
All CVs must be submitted in the English language for consideration.
Responsibilities
- Act as a PV contact/Local Safety Officer for DACH countries
- Communicate with Health Authorities and clients
- Ensure compliance with applicable local guidelines and regulation
- Collect, process, and reconcile about safety information
- Medical Information Requests handling
- Maintain and establish quality standards for local pharmacovigilance activities
- Ensure weekly monitoring of local literature review
- Participate in inspection and/or audits
- Ensure the survey and monitoring of national pharmacovigilance regulations
- Development and implementation of local standard operation procedures (SOPs)
- Creation and Provision of PV Training
Requirements
- Biologist, Pharmacist, Medical Doctor, or other life science degree
- 2-year experience in Local Pharmacovigilance activities in DACH region
- Fluent English and native German
- Computer literacy (MS Office), experience with PV databases
- Strong organizational and time management skills
- Ability to work independently and in a team
Benefits
- Professional growth and career opportunities
- International team and environment
- Bonus based on annual performance
- Personal accident and business trip insurance
- Additional health insurance
- Remote/home-based position
- Rewarding referral policy
- Workplace establishment allowance
- Team building, global meetings, B active events
- Role:
- Pharmacovigilance Specialist DACH region
- Job Type:
- Full Time
Company profile
Biomapas
biomapas.comBiomapas is a pan-European pharma services provider and full-service Clinical Research Organisation offering worldwide pharmacovigilance and medical information services, along with clinical development and regulatory affairs capabilities. It has worked across Europe, CIS/EAEU and MENA for over 20 years, helping clients meet timelines and milestones in their development programs. Its leadership includes Xavier Duburcq, who previously served as Chairman and CEO of ProductLife Group.