Senior Pharmacovigilance Specialist

Biomapas Group; United States; Remote; USD 69,000 - 104,000; Full time

Benefits offered by this job

Annual bonus

Remote-friendly work environment

Health insurance

Travel insurance

Referral program

Job summary

Biomapas is seeking a Sr. Pharmacovigilance Specialist to support global PV activities. The role offers remote work from any EU country and requires strong PV experience and English fluency.

You will act as PM or deputy PM, oversee KPIs, update SOPs, and ensure regulatory PV readiness across regions. The position emphasizes independence, teamwork, and career growth within an international team.

Qualifications

• 4-year experience in global Pharmacovigilance activities.
• Fluent English required.
• Degree in biology, pharmacy, medicine, or life sciences.
• Proficient in MS Office; PV databases experience is a plus.

Responsibilities

• Act as Project Manager or deputy PM for assigned PV projects.
• Forecasting and budget planning for the QPPV Office.
• Update SOPs and serve as PV SME in company processes.
• Maintain KPI reports and core PV activities for partners.
• Manage PV systems and projects (pre- and post-authorization).

Skills

Global Pharmacovigilance experience

Fluent English

MS Office proficiency

PV databases knowledge

Education

Life science degree

Tools

Veeva Vault Safety

Job description

Join our global Pharmacovigilance team as a Sr. Pharmacovigilance Specialist.

SeniorPharmacovigilance Specialist is responsible forsupporting 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

• 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 communicationand relationship building skills across functional teams

• 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