Biomapas
via Workable
Senior Pharmacovigilance Specialist
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 20h ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 18d ago
The date the source published, not the day we noticed it (2026-08-28). Last seen at its source 2h ago.
Is it remote?
Marked remote on the employer's board
Their board carries a remote setting on this posting — a field they filled in, not wording we read. The location field names somewhere specific, which is usually where the team or the entity sits.
Who may apply?
Croatia, Bulgaria, Poland, Czechia, Slovakia, Greece
The description states no restriction of its own. This is the source's own tag.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
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workable employer's own board first seen 10d ago · last seen 2h ago
The listing
Join our global Pharmacovigilance team as a Sr. Pharmacovigilance Specialist.
Senior Pharmacovigilance Specialist is responsible for supporting global and local PV systems and ensuring compliance with all PV activities with international or local regulations. May overtake additional regional or local PV responsible person roles for simple PV systems.
The position is remote, home-based in any EU country.
All CVs must be submitted in the English language for consideration.
Responsibilities:
- Act as the Project Manager or deputy Project Manager for the assigned projects
- Perform accurate forecasting and contribute to budget planning, ensuring efficient functioning of the QPPV Office
- Update SOPs and act as a subject matter expert for PV in assigned company processes
- Maintain KPI reports and perform core and standard PV activities for assigned contractual partners.
- Manage Full or local Pharmacovigilance systems and projects (or part of them) and/or central pharmacovigilance activities (e.g. end-to-end case processing, Aggregate Safety Reports, Risk Management Plans and risk minimization activities) in both pre- and post-authorization setting (as applicable)
- Act as a customer contact point (where applicable), ensuring consistent communication and escalation management across assigned projects
- Act as the appointed EU QPPV or deputy EU QPPV in accordance with a separate QPPV Job Description (if applicable)
- Ensure high-quality performance of PV services in assigned region/country and timely communication with Health Authorities
- Ensure inspection/audit readiness and finding remediation
Requirements
- Biologist, Pharmacist, Medical Doctor, or other life science degree
- 4-year experience in global Pharmacovigilance activities
- Fluent English
- Computer literacy (MS Office), experience with PV databases (Veeva Vault Safety experience is an advantage)
- Strong organizational and time management skills
- Ability to work independently and in a team
- Strong organization, prioritization, and time management with reliable delivery of commitments
- Strong communication and relationship building skills across functional teams
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
- Rewarding referral policy
- Workplace establishment allowance (fully remote)
- Team building, global meetings, B active events