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Local Contact for Pharmacovigilance with Estonian and English language

18 LOCATIONS (OTHER)HYBRIDPOSTED: 6/24/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
Iqvia

ROLE DEFINITION & RESPONSIBILITIES

Local Contact for Pharmacovigilance with Estonian and English language

As the Local Contact for Pharmacovigilance , you will act as local contact for Pharmacovigilance for customers requiring the services for their product(s). This role can be conducted either Home Based / Hybrid / Office based from anywhere in Europe - the choice is yours.

RESPONSIBILITIES

Respond fully and promptly to requests from Competent Authorities to evaluate the benefits and risks of a medicinal product to include information regarding sales or prescriptions or post-authorization of safety studies of medicinal products.
Remain up to date and aware of any changes in local regulatory requirements; verifies the necessary mechanisms and regulatory measures adopted for safety reasons and the risk management plans are carried out.
Establish and maintain a thorough understanding of each project’s budget and scope of work (SOW); set up and maintain project materials such as project files, forms, templates.
Provide regular reports to project manager on project metrics, SOW changes, customer requests or concerns; communicate and document project issues to project team members and department management in a timely manner;
Communicate regular monthly updates to the EU QPPV/designee & complete regulatory reports as required.
Support pharmacovigilance operations as required.

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

· Bachelor's degree in a life-science, medicine, pharmacy or nursing or educational equivalent.

· 3 years of prior relevant experience including experience managing clinical trial safety/post-marketing safety; or equivalent combination of education, training and experience.

· Excellent written and verbal skills in English (min. C1) and Estonian language (min. C2 / native).

In-depth knowledge of applicable global, regional and local regulatory requirements, International Conference on Harmonization (ICH) guidelines, and relevant Standard Operating Procedures (SOPs).
Very good knowledge of the pharmacovigilance legal framework in Estonia.
Maintain an overview of the safety profile of the product and factors that may affect the benefit/risk balance of a product.
Demonstrate an understanding of compliance and of quality management systems.

#LI-Remote   #LI-Hybrid   #LI-Onsite

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

REQUIRED VERIFIED SKILLS

Very good knowledge of the pharmacovigilance legal framework in Estonia.

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting
Salary for this Local Contact for Pharmacovigilance with Estonian and English language position is competitive and aligned with industry standards for this location.

ORGANIZATION CONTEXT & CULTURE

IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services (CRO) to the life sciences industry. The company helps pharmaceutical, biotech, and medical device clients accelerate the development and commercialization of new medical treatments through its extensive data, technology, and human expertise. Their offerings span from clinical trial design and execution to real-world evidence and commercial effectiveness.

TEAM SIZE: 87,000+ employees
INDUSTRY: Healthcare Technology & Contract Research

EXPECTED CAREER ROADMAP

PV Associate ➔ Senior PV Specialist ➔ PV Team Lead ➔ Pharmacovigilance Manager / Director.

APPLICATION ADVISORY

Ensure your resume clearly showcases experience with: Very good knowledge of the pharmacovigilance legal framework in Estonia.. Prepare real-world examples demonstrating these skills for the interview.
RECOMMENDED TRAINING
1/5
Industry Essentials of Pharmacovigilance

Industry Essentials of Pharmacovigilance

READY TO SUBMIT?

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