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Medical Writer III (Pharmacovigilance)

Ergomed


Job Location:

Belgrade - Serbia

Monthly Salary: Not provided by the employer
Posted: 24 October 2026 (2 days ago)
Application Deadline: 21 January 2027
Vacancies: 1 Vacancy

Job Summary

We are looking for an experienced pharmacovigilance medical writer to join our growing medical writing team.

What Were Looking For: A highly motivated and detail-oriented medical writer who combines strong regulatory writing expertise with a client-focused mindset and a passion for developing others. You will play a key role in delivering high-quality regulatory documents strengthening client relationships and supporting the growth of the wider team. The Medical Writer will be responsible for medical writing including:

Key Responsibilities:

  • Author review and quality check a range of regulatory and pharmacovigilance documents including:
    • PSURs/PBRERs
    • PADERs
    • ACOs
    • DSURs
    • Risk Management Plans (RMPs)
  • Ensure documents are scientifically accurate regulatory compliant and delivered within agreed timelines.
  • Collaborate with cross-functional teams to analyse interpret and present safety data effectively.
  • Act as a trusted point of contact for clients supporting project delivery and fostering strong working relationships.
  • Provide guidance mentoring and knowledge sharing to junior medical writers to support their professional growth and development.
  • Contribute to process improvements and the continuous enhancement of medical writing quality standards.

Qualifications :

  • MD pharmacy or Life Science degree (Masters or PhD is desirable)
  • Minimum 2 years experience in Medical Writing and associated fields (case processing signal detection or risk management) ideally within a CRO environment 
  • Ability to manage multiple and varied tasks and prioritize workload with attention to detail
  • Ability to effectively train and mentor Associate Medical Writers
  • Must be a strong team player
  • Fluency in English an additional language is a benefit

Additional Information :

When you join Ergomed Group you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. Youll join a passionate and collaborative team of experts in clinical research pharmacovigilance and quality consulting.  

We are diverse in many ways yet our values unite us. Our values are how we work not words on a wall. If they sound like you you will feel at home here. 

  • Quality: we hold ourselves to the standard patients deserve. 
  • Integrity and trust: we do the right thing especially when it is hard. 
  • Drive and passion: we care about the outcome because someone is waiting on it. 
  • Agility and responsiveness: we move quickly because patients cannot wait. 
  • Belonging: everyone is welcome and every voice counts. 
  • Collaborative partnerships: we go further by going together. 

We look forward to welcoming your application. 


Remote Work :

Yes


Employment Type :

Full-time


About Company

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Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance solutions, integrated under the PrimeVigilance brand and a full range of high-quality clinical research and trial management services under the Ergomed Clinical Research brand. ... View more

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