Senior Pharmacovigilance Specialist
B
BiomapasPharmacovigilance
Croatia. Bulgaria. Poland. Czechia. Slovakia. Greece. The position is remote, home-based in any EU country.Full-TimeSenior
Salary not disclosed
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Job Details
- Languages
- Fluent English
- Experience
- 4-year experience in global Pharmacovigilance activities
- Required Skills
- MS Office
Requirements
- Life science degree (Biologist, Pharmacist, Medical Doctor, or similar).
- 4 years of professional experience in global Pharmacovigilance activities.
- Fluent in English (CVs must be in English).
- Computer literacy in MS Office.
- Experience with PV databases (Veeva Vault Safety is a plus).
- Strong organizational, prioritization, and time management skills.
- Ability to work independently and as part of a team.
- Strong communication and relationship-building skills.
Responsibilities
- Act as the Project Manager or deputy Project Manager for assigned projects.
- Perform accurate forecasting and contribute to budget planning for the QPPV Office.
- Update SOPs and serve as a subject matter expert for PV processes.
- Maintain KPI reports and perform core and standard PV activities for contractual partners.
- Manage full or local Pharmacovigilance systems and projects, including case processing, Aggregate Safety Reports, and Risk Management Plans.
- Act as a customer contact point, ensuring consistent communication and escalation management.
- Appointed as EU QPPV or deputy EU QPPV as applicable.
- Ensure high-quality PV services in the assigned region and maintain timely communication with Health Authorities.
- Ensure inspection and audit readiness and manage finding remediation.
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