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Pharmacovigilance Manager, Baltics and Ukraine
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AbbVie

Pharmacovigilance Manager, Baltics and Ukraine

Onsite Vilnius, Lithuania Full Time
Posted 5 hours ago
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powertofly approved What AbbVie Has to Offer:

Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.

Job Details


Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.


Job Description

AbbVie is looking for a Pharmacovigilance Manager for the Baltics & Ukraine, based in Lithuania. In this role, you will serve as the Affiliate Safety Representative for the Baltics and Ukraine and will be part of the Medical Department within the IMA (International Medical Affairs) organization. Additionally, you will act as AbbVie’s PV contact person at the national level (Local Safety Representative) in Lithuania for communication with the National Regulatory Agency. For all pharmacovigilance-related matters, this position also has a dotted-line indirect reporting relationship to the AbbVie’s EU QPPV.

In this position you are responsible to maintain oversight of the performance of all activities that fulfil local and applicable regional PV regulations, including those performed by the Regional PV Team and/or outsourced partners, in collaboration with Regional PV Leaders who oversee day-to-day operational PV activities.

You partner with the Regional PV Team to ensure Affiliate PV System procedure(s) aligns with corporate PV procedures and complies with local and regional PV regulations.

Additionally you are responsible to:

  • Maintain oversight of the PV system and ensures that processes, procedures and systems are in place for intake, processing, follow up, translation and reconciliation of adverse events and other safety information reportable to GPS (Global Patient Safety) from spontaneous and solicited sources as well as from clinical studies.
  • Serve as the Affiliate Lead and point of contact for affiliate PV audits and Regulatory Authority PV inspections, demonstrating understanding of the overall AbbVie PV system and how Global PV processes and the GPS Regional PV Team are set-up and structured, supporting the fulfilment of local legal requirements.
  • Act as key safety advisor for affiliate cross-functional partners on safety topics. Leads product safety communication and education initiatives for local cross-functional teams on major PV topics and on local data sources.
  • Lead local risk management activities in alignment with local regulations with the Affiliate Medical Director.
  • Act as key driver in the generation and interpretation of safety evidence across the product lifecycle.
  • Drive AbbVie PV advocacy efforts through strong internal and external collaboration including engagement with local trade associations, industry network, and with Regulatory Agencies.

Qualifications

The ideal candidate has a medical, pharmacy or life-sciences degree (or equivalent) and at least three years’ experience working in the pharmaceutical industry in a pharmacovigilance role is required. 

You have:

  • Adequate theoretical knowledge and practical experience of PV activities and system under purview (as stipulated in local guidance) and sound understanding of the regulatory and PV monitoring requirements for assigned territory(ies) that comply with any specific training requirements mandated by relevant regulatory agencies.
  • Excellent written and spoken communication and presentation skills.
  • Fluency in written and oral English is essential to facilitate communications with GPS, Area/Regional Medical and other headquarters functions.
  • Fluency in written and oral local language is a requirement to facilitate communications within the affiliate medical department, and with the National Regulatory Agency.
  • High customer orientation.
  • Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity.
  • Strong scientific acumen and the ability to understand and apply scientific concepts effectively.
  • Sound judgment, strong planning and organizational skills, and the ability to get things done. Demonstrated strong sense of urgency.
  • Valid driving license.

Additional Information

This position is based at our office in Vilnius.

Please submit your application, in English, at your earliest convenience, applications will close on the 5th March 2026.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Company Details
AbbVie
 Chicago, IL, United States
Work at AbbVie

Together, we break through We believe the paths we take to achieving our breakthroughs matter. At AbbVie, every one of our 50,000 employees is a... Read more

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