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Senior Medical Writer (Line Management Experience Required)

Prime Vigilance
Prime Vigilance
0-2 years
Not Disclosed
Aachen, Abbott Park, Aberdeen, Europe
10 Oct. 9, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

🧠 Position: Senior Medical Writer (Line Management Experience Required)

📍 Location: Delhi, India
🏢 Department: Medical Writing
🕓 Employment Type: Full-Time


🏢 Company Overview – PrimeVigilance (Part of Ergomed Group)

Founded in 2008, PrimeVigilance is a specialized pharmacovigilance service provider and part of the Ergomed Group. With offices across Europe, North America, and Asia, we deliver comprehensive services in:

  • Medical Information

  • Pharmacovigilance

  • Regulatory Affairs

  • Quality Assurance

We are proud to be a global leader in pharmacovigilance, supporting small to large pharmaceutical and biotechnology partners across all therapeutic areas, including medical devices.

At PrimeVigilance, we strongly value:

  • Employee growth and well-being

  • Work-life balance

  • Continuous learning and professional development

Join us in our mission to make a positive impact on patients’ lives worldwide.


🧾 Job Summary

The Senior Medical Writer role offers a unique opportunity to advance your career in drug safety and regulatory medical writing. The position requires prior experience in pharmacovigilance medical writing and line management.


🔹 Key Responsibilities

  • Independently author, edit, and review regulatory and clinical documents (e.g. PBRERs, DSURs, RMPs, and other lifecycle documents).

  • Ensure high-quality, compliant documentation aligned with internal and external standards.

  • Actively participate in training, quality system maintenance, and the development of internal templates and SOPs.

  • Provide support in pharmacovigilance operations related to medical writing.

  • Maintain continuous learning and self-development in pharmacovigilance and medical writing.

  • Manage and mentor a team of junior/associate medical writers to ensure quality output and skill development.


🎓 Qualifications & Experience

  • Proven experience in pharmacovigilance medical writing, including authoring of PBRERs, DSURs, and RMPs.

  • Life Science degree (or equivalent medical/nursing qualification).

  • Strong ability to prioritize and manage multiple tasks with attention to detail.

  • Demonstrated experience in training and mentoring junior writers.

  • Advanced English proficiency (written and verbal).


🌍 Diversity & Inclusion

We are committed to fostering a workplace built on:

  • Diversity, Equity, and Inclusion

  • Human-first collaboration

  • Respect for all cultures, genders, and backgrounds

Our people are our greatest strength, driving innovation and improving lives globally.


💡 What We Offer

  • Comprehensive training and career development opportunities.

  • Strong focus on personal and professional growth.

  • Friendly, supportive, and collaborative work culture.

  • Opportunity to work with a global team — English is our company language.


💎 Our Core Values

  • Quality

  • Integrity & Trust

  • Drive & Passion

  • Agility & Responsiveness

  • Belonging

  • Collaborative Partnerships