Senior Pharmacovigilance Specialist

Biomapas; Poland; On-site; PLN 282,000 - 391,000; Full time

Benefits offered by this job

Remote/home based

International team

Bonus based on annual performance

Health insurance

Job summary

Biomapas is seeking a Sr. Pharmacovigilance Specialist to join our global PV team. The role supports global and local PV systems and ensures compliance with PV activities under international and local regulations.

This remote, EU-based position offers exposure to QPPV duties and diverse regional PV responsibilities. Applicants must hold a life science degree, have 4+ years in global PV, and be fluent in English.

Qualifications

• Requires a life science degree
• At least 4 years of global Pharmacovigilance experience
• Fluent English is mandatory

Responsibilities

• Act as Project Manager or deputy PM for assigned PV projects
• Forecasting and budget planning for QPPV Office
• Update SOPs and provide PV subject-matter expertise
• Maintain KPI reports and perform core PV activities for partners
• Manage PV systems/projects including case processing, RMPs and PSURs across regions

Skills

Fluent English

Veeva Vault Safety

MS Office

Time management

Communication

Teamwork

Education

Life science degree (Biologist, Pharmacist, Medical Doctor)

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

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 communicationand 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