Join Biomapas Group as a Pharmacovigilance Project Manager to oversee strategic/key accounts, manage team, and ensure high quality local performance in Pharmacovigilance.
Requirements
- Life science degree
- 5-year experience in Pharmacovigilance
- Experience with end-to-end case processing of clinical trials
- Oncology background preferred.
- Veeva Vault handling preferred
- Fluent English
- Excellent knowledge of international regulations (ICH, EU GVP Modules)
- Strong computer literacy with intensive experience with safety data bases and MS Office
- Demonstrated ability to set up and implement drug safety strategies, develop PV related procedures, elevate and resolve issues
- Strong communication, organizational and time management skills
- Ability to work independently and in a team
Benefits
- Professional growth and career opportunities
- International team and environment
- Rewarding business referral policy
- Employee referral policy
- Flexible working hours
- Remote working