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Medical Writer Senior - Vaf 189

7+ years
Not Disclosed
10 March 19, 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

Medical Writer Senior – VAF 189
Location: Paris (Hybrid)
Department: Life Cycle - Safety and Vigilance
Contract Type: Permanent

About ProductLife Group:

ProductLife Group (PLG) is dedicated to improving human health by delivering regulatory compliance services to ensure the safe and effective use of medical solutions. For nearly 30 years, PLG has supported clients throughout the entire product life cycle, combining local expertise with a global reach across more than 130 countries. PLG provides consulting and outsourcing services in regulatory affairs, quality and compliance, vigilance, and medical information for both established products and innovative therapeutics.

With revenue growth from €25 million in 2020 to €210 million in 2024, and an ambitious goal of reaching €600 million by 2028, PLG continues to grow through an active M&A strategy, having closed 23 build-ups since 2020.

Responsibilities:

  • Act as LRPPV in France and serve as the single point of contact with French health authorities.

  • Provide backup for local PV in France when required.

  • Handle signal detection, off-label use reports, and aggregate reports (DSUR, PSUR, RMP, ACP, etc.).

  • Write and maintain PSMF and SDEA, and engage in regulatory intelligence activities.

  • Prepare to assume deputy and EU QPPV roles in the future.

  • Participate in audits and health authority inspections on behalf of PLG clients.

  • Serve as Pharmacovigilance Responsible Person for France for selected clients.

  • Lead and manage safety writing tasks, including PSUR, PBRER, ACO, CES, DSUR, and signal detection.

  • Coordinate with internal and external stakeholders, including MAHs and ‘exploitants.’

  • Ensure compliance with safety and quality standards.

  • Manage project timelines, reporting on progress and performance.

Profile:

Education:

  • Pharmacist or Physician residing in France (mandatory to meet French PV regulatory requirements).

Experience:

  • Minimum of 7 years of experience in PV activities, particularly in safety writing.

  • Previous role as Deputy QPPV and/or RPV.

  • Experience working with multiple clients and different PV systems.

  • Direct participation in inspections by health authorities.

Languages:

  • French and English proficiency.

Technical Skills:

  • Extensive experience in PV and in-depth knowledge of health and safety regulations (GVP and BPPV).

  • Knowledge of case management processes.

  • Strong safety writing skills (drafting, quality control, and medical review).

  • Proficiency in safety database software.

  • Expertise in MS Office and pharmacovigilance tools.

  • Understanding of customer products and services.

  • Audit and inspection experience.

Soft Skills:

  • Strong leadership and team management skills.

  • High rigor, reliability, and accountability.

  • Effective communication skills.

  • Strong time and priority management.

  • Excellent organizational and multitasking abilities.

  • Business-oriented mindset.