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Senior Pv Associate - Clinical Trials Experience Required

3+ years
€16,000 – €22,000
10 June 20, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior PV Associate – Clinical Trials Experience Required
Location: Belgrade, Serbia
Employment Type: Full-time
Department: ICSR Management

Company Overview:
PrimeVigilance, part of Ergomed PLC, is a globally recognized mid-sized pharmacovigilance service provider founded in 2008. With a global team across Europe, North America, and Asia, we deliver high-quality services in Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance. We proudly support clients of all sizes and therapeutic focuses—including medical devices—ensuring compliance and patient safety.

We believe that professional growth, well-being, and a healthy work-life balance create a stronger and more effective team. Join us in our mission to make a lasting difference in patient lives.

Job Summary:
We are seeking a Senior PV Associate with clinical trials case processing experience to join our growing team in Belgrade. This role involves performing and supporting contracted pharmacovigilance activities with a strong focus on Individual Case Safety Report (ICSR) management across a variety of projects—ranging from small-scale clinical trials to large post-marketing surveillance programs.

Key Responsibilities:

  • Process Individual Case Safety Reports (ICSRs) from all sources—especially clinical trials—in compliance with regulatory requirements, internal SOPs, and client-specific timelines.

  • Perform tasks related to triage, data entry, quality review, and submissions.

  • Conduct reconciliation of received safety reports.

  • Collaborate within multidisciplinary project teams.

  • Work under the guidance and mentorship of more experienced colleagues.

Candidate Requirements:

  • Degree in Life Sciences or a health-related field (e.g., Chemistry, Biology, Biotechnology, Veterinary Science).

  • Previous pharmacovigilance experience required, particularly in clinical trial case processing.

  • Experience with Oracle Argus safety database is mandatory.

  • Prior submission experience is preferred.

  • Demonstrated passion for learning and contributing to patient safety.

  • Strong organizational, multitasking, and attention to detail skills.

  • Effective time and issue management skills.

  • Excellent communication and interpersonal abilities.

  • Advanced English proficiency (minimum B2 level), both spoken and written.

Why Join PrimeVigilance:

  • Work in a fast-growing, dynamic team with global reach.

  • Opportunity for rapid career progression.

  • Multicultural and inclusive workplace with English as the company language.

  • Focus on personal and professional development.

  • Access to extensive PV training programs, both internal and international.

  • Friendly and supportive work culture, with regular team events.

Core Values:

  • Quality

  • Integrity & Trust

  • Drive & Passion

  • Agility & Responsiveness

  • Belonging

  • Collaborative Partnerships

Estimated Salary: €16,000 – €22,000 annually (based on Serbian industry standards for senior PV roles with clinical trial experience)

Slug: senior-pv-associate-clinical-trials-belgrade-serbia