Senior Pharmacovigilance Specialist

BiomapasAustria, Belgium + 25 more

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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

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Senior Pharmacovigilance Specialist

BiomapasAustria, Belgium + 25 more

Apply now

Opens the original posting.

Apply now

Share job

Copy link or share on social media.

Apply on the original site

Companies in this catalog do not charge applicants. Never send money to apply.

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
Originally posted on Himalayas

Apply now

Opens the original posting.

Apply now