Medical Writer - Future roles (UK)

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. We build a wide range of business‑critical services that support our vision of Shortening the Distance from Lab to Life® and value the talents of our 29,000 employees across 110 countries.

We are passionate about developing our people through career development, technical and therapeutic area training, peer recognition, and a total rewards program. We are committed to our Total Self culture – where you can authentically be yourself and take care of our people. We continuously build the company we all want to work for by fostering diversity of thoughts, backgrounds, cultures, and perspectives so everyone feels they belong.

Data show our work across 73,000 sites with 675,000+ trial patients and involvement in 94% of all novel FDA‑approved drugs and 95% of EMA‑authorized products.

• Compiles, writes, edits, and coordinates medical writing deliverables that present scientific information clearly and accurately under moderate supervision.
• Completes a variety of documents such as clinical study protocols, protocol amendments, clinical study reports, patient narratives, and investigator brochures.
• Adheres to regulatory standards (ICH E3, company SOPs, client standards, approved templates, authorship requirements, style and formatting guides) to complete projects on time and within budget.
• Coordinates quality and editorial reviews, ensuring source documentation is managed, leading document reviews, resolving client comments, and reviewing statistical analysis plans and table/figure specifications for content, grammar, format, and consistency.
• Builds and maintains good relationships with clients, department heads, and peers to produce high‑quality deliverables.
• Performs online clinical literature searches while complying with copyright requirements.
• Identifies and proposes solutions to resolve document issues, escalating as appropriate.
• Engages in ongoing professional development to stay current on industry standards and client expectations.
• Conforms to budget specifications, working within the budgeted hours and communicating status and changes to leadership.
• Completes required administrative tasks within specified timeframes and handles other duties as assigned.
• Travel may be required up to 25% of the time.

This posting is intended for an upcoming opportunity rather than a live role. By expressing interest you will be added to our talent pipeline and considered should the role become available.

Tasks, duties, and responsibilities listed in this job description are not exhaustive. Tasks may be assigned at the company’s discretion, and equivalent experience may be considered. Language herein complies with all applicable legislation, including the EU Equality Directive and the Americans with Disabilities Act, which we have committed to comply with by providing reasonable accommodations.

Medical writer on clinical study or regulatory project teams. Writes, edits, and coordinates content for clinical/regulatory documents to ensure high‑quality completion of all assigned writing projects.