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Senior Specialist, Regulatory And Pharmacovigilance

3+ years
€60,000 – €85,000 annually
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 Specialist, Regulatory and Pharmacovigilance
Location: Remote
Employment Type: Full-time
Department: Regulatory and PV Network

Company Overview:
PrimeVigilance, a part of the Ergomed Group, is a mid-sized pharmacovigilance service provider founded in 2008. We operate globally with teams across Europe, North America, and Asia, offering specialized services in Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance. Our client base spans from small biotech startups to large pharmaceutical companies across all therapeutic areas, including medical devices.

We pride ourselves on a culture of professional development, mental well-being, and strong work-life balance—core values that translate into exceptional service for our clients and meaningful careers for our employees.

Job Summary:
The Senior Specialist, Regulatory and Pharmacovigilance plays a dual role—driving strategic and operational deliverables for regulatory and PV projects and serving as the Local Contact Person for Pharmacovigilance in the designated country. The role requires strategic thinking, cross-functional coordination, and a hands-on approach to regulatory compliance and client engagement.

Key Responsibilities:

  • Act as Local Contact Person for Pharmacovigilance in the assigned country.

  • Lead and represent functional areas in medium/high complexity projects, ensuring timelines and quality standards are met.

  • Develop and execute project strategies, operational plans, and key documentation with senior oversight.

  • Provide regulatory guidance and proactively identify and mitigate risks.

  • Resolve issues and support performance troubleshooting on assigned projects.

  • Maintain and review documentation for Local Contact Persons (LCPs), including CVs, training records, and reports.

  • Ensure proper training assignment and compliance of LCPs.

  • Track budgets, hours, and project deliverables, and escalate out-of-scope issues.

  • Assist in proposal development, budgeting, and attend BD meetings when required.

  • Manage client billing and review vendor invoices.

  • Mentor and train junior staff, fostering a culture of continuous learning.

  • Build and maintain professional relationships with internal and external stakeholders.

  • Monitor and share regulatory legislative changes and maintain intelligence databases.

  • Support audits/inspections and act as departmental representative for projects.

  • Track and report on LCP performance indicators.

  • Provide input for SOPs, working practices, and department-wide initiatives.

Candidate Requirements:

  • Bachelor’s Degree in Chemistry, Life Sciences, Nursing, or equivalent experience.

  • Strong background in the pharmaceutical, CRO, or regulatory environment.

  • In-depth understanding of ICH GCP/GVP and national regulatory requirements.

  • Pharmacovigilance training and/or experience in line with local regulatory expectations.

  • Fluency in English (written and spoken); proficiency in the local official language is essential.

  • Proficiency in German, French, or Italian is a plus.

  • Strong organizational, planning, and interpersonal skills.

  • Detail-oriented and comfortable working in fast-paced and dynamic environments.

Why Join PrimeVigilance:

  • Comprehensive training and career development programs.

  • Emphasis on personal growth and internal mobility.

  • Collaborative and supportive work culture.

  • Work in a global team with English as the corporate language.

  • Be part of an organization driven by values:

    • Quality

    • Integrity & Trust

    • Drive & Passion

    • Agility & Responsiveness

    • Belonging

    • Collaborative Partnerships

Estimated Salary: €60,000 – €85,000 annually (depending on location and experience)