Senior Pharmacovigilance Specialist

Company shown to members 🔒 · Remote · Czech Republic, Greece, Bulgaria +1 only

Czech Republic, Greece, Bulgaria +1 onlySeniorPublished 28 August 2026Check carefully

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First recorded by Psst: 12 October 2026. Your first 3 jobs are free to apply to (the first right away, 2 more with your email). After that, the company and the apply link are for Psst members, from $4.99 for 7 days.

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The 20-second read

Experience
Senior
Where you can live
Czech Republic, Greece, Bulgaria +1 only
Languages
English
Skills and tools
forecasting, compliance, time management
Job type
Full-time

Read from the ad by Psst's rules. Check the full ad below before applying.

Job details

Where you can work
Czech Republic, Greece, Bulgaria, Croatia
Employment type
Full-time
Advertised pay
Not stated by the employer
Experience
Senior
Employer publication date
28 August 2026
First recorded by Psst
12 October 2026
Last checked at the source
8 November 2026

About the job

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

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