Sponsor-Dedicated Senior Medical Writer

Syneos Health, Inc.

United Kingdom

On-site

GBP 60,000 - 90,000

Full time

8 days ago

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Job summary

Syneos Health, Inc. is seeking a Senior Medical Writer to lead the preparation and delivery of medical writing deliverables for sponsor-dedicated programs across the UK, Poland, Spain and Serbia.

The role requires coordinating with data management, biostatistics, regulatory affairs, and medical affairs to ensure accurate, regulatory-compliant documents. You will oversee manuscript drafting, study reports, and regulatory submissions while mentoring junior writers and ensuring adherence to ICH/E3

Qualifications

  • 3-5 years of relevant experience in science, technical, or medical writing.
  • Experience in biopharmaceutical, device, or contract research organization industry required.
  • Strong understanding of FDA and ICH regulations, other regulatory guidelines, and/or good publication practices strongly required.
  • Experience writing relevant document types required.
  • Extensive knowledge of English grammar and ability to communicate clearly; familiarity with AMA Manual of Style.

Responsibilities

  • Leads the clear and accurate completion of medical writing deliverables for studies, coordinating activities across departments with minimal supervision.
  • Produces documents such as clinical study protocols, summaries, safety reports, and journal manuscripts.
  • Adheres to regulatory standards and company templates, ensuring on-time, on-budget delivery.

Skills

Medical writing
Regulatory knowledge
English proficiency
Scientific communication

Job description

Syneos Health, Inc. is seeking a Senior Medical Writer to lead the preparation and delivery of medical writing deliverables for sponsor-dedicated programs across the UK, Poland, Spain and Serbia.

The role requires coordinating with data management, biostatistics, regulatory affairs, and medical affairs to ensure accurate, regulatory-compliant documents. You will oversee manuscript drafting, study reports, and regulatory submissions while mentoring junior writers and ensuring adherence to ICH/E3

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