Join our global team as a Senior Pharmacovigilance Specialist in CIS region.
Senior Pharmacovigilance Specialist is responsible for assuring compliance with local and regional (Eurasian Union) Quality Management System and exchange relevant safety and pharmacovigilance information.
Responsibilities:
- Communicate with Health Authorities
- Ensure compliance with applicable local guidelines and regulation
- Collect, process and communicate of safety information
- Maintain and establish of pharmacovigilance system considering the EAEU GVP quality standards
- Ensure weekly monitoring of local literature review
- Participate in inspection and/or audits
- Create and regular maintain of EAEU PSMF
- Monitoring of EAEU Commission official website and newsletters
- Oversight and regular management of SDEAs
Requirements
- Biologist, Pharmacist, Medical Doctor, or other life science degree
- 3-year experience in Pharmacovigilance (preferable in EAEU QPPV and LSO roles)
- Fluent English
- 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
- Influenza vaccines
- Rewarding referral policy
- Workplace establishment allowance
- Flexible working hours
- Team building, global meetings, B active events
Kazakhstan
