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Pharmacovigilance Project Manager (Lcppv Responsibilities)- Germany Based

3+ years
Not Disclosed
10 April 24, 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

Job Title: Pharmacovigilance Project Manager (LCPPV Responsibilities)
Location: Remote (Germany based)
Employment Type: Full-time
Department: Project Management


About the Company:

PrimeVigilance, part of the Ergomed Group, is a specialized mid-size pharmacovigilance service provider established in 2008. With global presence across Europe, North America, and Asia, the company offers services in Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance. PrimeVigilance partners with pharmaceutical and biotechnology organizations of all sizes, delivering expert services across all therapeutic areas including medical devices.

The company emphasizes employee development, mental health, and work-life balance to foster a high-performance culture and ensure superior client service.


Job Responsibilities:

  • Serve as the primary contact for project-related matters, acting as the Local Contact Person for Pharmacovigilance (LCPPV)

  • Manage client expectations to ensure satisfaction and that deliverables meet or exceed expectations

  • Define project scope and objectives in accordance with signed client agreements

  • Plan project activities, establish deadlines, and define interim milestones

  • Prepare regular reports for both clients and PrimeVigilance management, including monthly reporting used for invoicing


Required Qualifications:

  • Proven experience in pharmacovigilance, including ICSR processing and quality review, aggregate reporting, literature screening, reconciliation, and SOP preparation

  • Previous project management experience in pharmacovigilance, preferably within a service provider or CRO setting

  • Degree in a healthcare or life sciences field

  • Strong communication skills and comfort in engaging with senior stakeholders in pharmaceutical organizations

  • Demonstrated leadership skills: planning, mentoring, meeting facilitation, communication, and problem-solving

  • Fluency in both English and German is mandatory


What We Offer:

  • Internal training and career development opportunities

  • Strong focus on personal and professional advancement

  • Friendly, supportive global team environment

  • Work with international colleagues, with English as the company language

  • A culture centered around core values:

    • Quality

    • Integrity & Trust

    • Drive & Passion

    • Agility & Responsiveness

    • Belonging

    • Collaborative Partnerships