[Hiring] Senior Medical Writer @Kinetix Health Group

Role Description

The Senior Medical Writer is responsible for developing and delivering scientifically accurate content aligned with client objectives, meeting specifications, budget, and schedule.

• Develop and maintain knowledge of relevant therapy areas, including product/competitor awareness, key trial data, messaging, and terminology.
• Participate in, and when necessary lead, client meetings on scientific and editorial project aspects.
• Liaise with and brief KOLs as required; act as the point of contact for clients and KOLs on specified projects.
• Coach, mentor, or line manage writers as appropriate, providing opportunities to learn and apply skills to future work.

Main duties include:

• Research, write, and review med ed and communications materials to the highest scientific and grammatical standards, including manuscripts, abstracts, posters, presentations, print items, and multimedia.
• Ensure accurate interpretation and incorporation of amendments from NexGen staff, clients, KOLs, and other stakeholders.
• Maintain in-depth knowledge of therapy areas, markets, audiences, and key messages; contribute to strategic communication plans and monitor relevant media/pharma developments.
• Assist managers by forecasting workload/resources, and brief/review freelance writers to ensure smooth workflow and timely delivery.
• Ensure adherence to agency processes, regulatory, and compliance guidelines; coach junior staff accordingly.
• Attend congresses or client meetings as team lead or independently; provide medical writing or client support and debrief teams afterward.
• Collaborate with client services to maximise organic growth within existing accounts.
• Contribute creative med ed and communication concepts for business development and ongoing programmes.
• Support new business activities, including pitch presentations showcasing agency expertise.
• Act as senior scientific services contact for specified accounts; liaise with clients, healthcare professionals, and external bodies, leading client & KOL meetings to develop scientific content.
• Assist PMW and STLs to ensure timely project delivery.
• Check and sign off final materials for print/production.
• Provide guidance on scientific direction and creative design input.
• Advise on budget and schedule development, maintaining awareness of required writing hours and overall budget.
• Coach and develop junior writers; review and QC projects to ensure consistent quality.
• Support recruitment of scientific services staff, including CV screening, writing tests, interviews, and decision-making.

Qualifications

• Degree or higher in biomedical science.
• Several years’ med comms agency experience with strong teamwork.
• Desirable: Previous managerial experience.
• Excellent attention to detail, grammar, and syntax.
• Strong project management, organisational skills, and commercial awareness.
• Excellent interpersonal and communication skills; able to work under pressure.
• Proficient in MS PowerPoint and Word.
• Solid understanding of drug development processes and US/EU regulations.
• High-quality scientific writing; able to adapt content for different audiences.
• Ability to coach junior writers, review content, and provide constructive feedback.
• Willingness to travel (UK/international) for NexGen or client meetings.

Key Result Areas

• Delivery of high-quality med ed and communication projects that meet specifications, deadlines, and budgets.
• Drive clear, proactive communication across teams to ensure timely action on projects, opportunities, and ideas.
• Ensure adherence to healthcare compliance laws, guidelines, and agency/client SOPs.
• Quality assurance of content produced by scientific services staff.
• Coaching, ongoing development, and line management of junior staff.