Senior Medical Writer

Bamboo Medical Communications
Surrey
9 months ago
Applications closed

Related Jobs

View all jobs

Senior Medical Writer - PBRER, DSUR, Protocol

Senior Design Engineer - Medical Devices

Global Medical Director

Senior Regulatory Affairs Specialist

Senior Regulatory Affairs Specialist - Hybrid (Warrington

Senior Project Manager, R&D: Drug Development

THE COMPANY


At Bamboo Medical Communications we are dedicated to shaping the future of healthcare communications. Our talented and vibrant team supports our clients in shining light on cutting-edge treatments that make life-changing impact on thousands of patients all over the world.[AL1]We provide tailored expertise in Medical Communications, Medical Education, Medical Affairs, and Medical Events for pharmaceutical and medical device companies across a huge variety of therapy areas.


We are a dynamic and innovative agency committed to advancing healthcare by creating clear, engaging, and impactful content for healthcare professionals and patients across the globe.


Job Title:Senior Medical Writer

Reports to:Medical Director

Job type:Full-time; Hybrid; minimum of 1 day a week in office

SALARY:£43,000 - £50,000 depending on experience


ROLE DESCRIPTION:

We are looking for an experienced Senior Medical writer, who likes to push the boundaries of what is possible within the realm of science communication. Creativity and a talent for storytelling are a must.


This role is positioned within our Scientific Services Team, which covers a multitude of different disease areas. Loving science and keeping up with the newest research developments is in their DNA.


As part of your role, you will be expected to create engaging scientific content for a broad range of materials, including training tools (e.g. e-learning modules, interactive slide decks), publications (e.g. manuscripts, abstracts and posters), meeting materials (e.g. agendas, slides and reports) and HCP/patient support materials (e.g. whitepapers, website copy, email campaigns, video/podcast scripts, animation storyboards). You are directly responsible for developing content that not only meets the client’s needs but also appeals to a variety of different target audiences (e.g. HCPs, patient carer and the wider pharmaceutical industry).


KEY RESPONSIBILITIES:

  • Content Creation:Independently review briefs and create scientifically accurate, engaging, and audience-appropriate materials that are clear, well-referenced, and meet high-quality standards.
  • Strategic Expertise:Build and maintain in-depth knowledge of relevant therapy areas to provide informed strategic insights, recommendations, and tailored solutions for clients and internal teams.
  • Project Coordination:Manage multiple projects across diverse therapy areas simultaneously, ensuring timely delivery of high-quality outputs while maintaining attention to detail.


  • Team Support:Actively mentor junior writers to support their professional growth and collaborate effectively with cross-functional teams to achieve shared goals.


MANDATORY QUALIFICATIONS:

  • Minimum of 3 years of experience as a Medical Writer in a commercial setting (e.g., medical communications agency, pharmaceutical company etc.).
  • Advanced Degree: A master’s or PhD in life sciences.
  • Strong understanding of medical terminology, clinical research/trial science and regulatory requirements.
  • Experience managing writing projects, timelines, and interacting with cross-functional teams.
  • Experience with document management systems, reference management tools (e.g., EndNote), and proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
  • Proficiency in Veeva PromoMats.
  • Understanding of the ABPI and EFPIA.
  • Self-motivated and proactive.
  • A keen eye for detail.
  • Ability to work independently and as part of a collaborative team.


We are looking for a passionate writer, who not only enjoys science but also loves writing.


APPLICATION PROCESS:

Interested candidates should submit a resume, covering letter and scientific and creative writing example to


Candidates must have the right to work in the UK and be able to attend the office at least one day per week.


Successful applicants will be contacted by email. The interview process will consist of a preliminary screening interview (virtual) followed by a writing assessment and interview at the Bamboo office.

Subscribe to Future Tech Insights for the latest jobs & insights, direct to your inbox.

By subscribing, you agree to our privacy policy and terms of service.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

New Biotech Employers to Watch in 2026: UK and Global Companies Transforming Life Sciences Careers

The biotechnology job market in the UK is entering a new phase—one defined by scientific breakthroughs, targeted investment, and a growing pipeline of innovative employers. For professionals browsing BiotechnologyJobs.co.uk, the key question is no longer just which companies exist, but which ones are scaling, hiring, and shaping the future of life sciences. In this article, we explore the new biotech employers to watch in 2026, focusing on UK-based startups, scale-ups, and international firms with a growing UK presence. These organisations have recently secured funding, partnerships, or strategic backing—strong indicators of hiring momentum in the months ahead.

CSL Behring Jobs UK: Careers, Salaries, Locations & How to Get Hired

CSL Behring is one of the world’s leading biopharmaceutical companies specialising in plasma-derived therapies, recombinant proteins, gene therapy, vaccines, and rare disease treatments. If you’re a UK job seeker looking for a career with real purpose, strong scientific standards, and long-term progression, CSL Behring roles can be an excellent fit, especially if you have experience in biotech, pharma manufacturing, quality, engineering, supply chain, clinical operations, regulatory, pharmacovigilance, or commercial. This guide is written for UK candidates who want to understand what CSL Behring jobs typically involve, which roles to target, where opportunities may be based, what skills recruiters look for, and how to tailor your application to stand out.

How Many Biotechnology Tools Do You Need to Know to Get a Biotech Job?

If you are trying to break into biotechnology or progress your career, it can feel like the list of tools you are expected to know is endless. One job advert asks for PCR, another mentions cell culture, another lists bioinformatics pipelines, automation platforms or GMP systems. LinkedIn makes it worse, with people sharing long skills lists that make you wonder if you are already behind. Here is the reality most biotech employers will not say out loud: they are not hiring you because you know every tool. They are hiring you because you understand biological systems, can work accurately and safely, follow protocols, interpret results and contribute reliably to a team. Tools matter, but only when they support those outcomes. So how many biotechnology tools do you actually need to know to get a job? The answer depends on the role you are targeting, but for most job seekers it is far fewer than you think. This article breaks down what employers really expect, which tools are essential, which are role-specific, and how to focus your learning so you look employable rather than overwhelmed.