Clinical Editor jobs
- MedComms ExpertsLondon W1W
- By combining scientific depth with human-centered storytelling and digital innovation, we help medical and scientific leaders communicate with clarity,…
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- NovartisLondon
- Proven experience in clinical development, clinical operations, or a similar environment (3–5 years).
- Strong expertise in clinical document management processes…
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- WileyRemote
- The Editor-in-Chief/Deputy Editor actively participates in the peer review process and decision-making for submitted manuscripts while ensuring adoption of best…
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- ParexelRemote
- Comprehensive understanding of clinical study conduct and contractual frameworks.
- Work with the Best: Collaborate with talented proposal specialists, sales…
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View similar jobs with this employerPublic Library of ScienceCambridge- Company pension
- Paid volunteer time
- Private medical insurance
- Experience in a research or clinical environment, publishing, or other relevant setting; experience in medical publishing strongly preferred.
- BDDrachten
- Waters collaborates with analytical laboratories around the world to advance the release of effective, high-quality medicines, assure the safety of food and…
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- BDDrachten
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- BioPhorumLondon
- A strong writer and editor, able to simplify and improve complex content.
- The Publications Coordinator will play a key role in managing BioPhorum’s publications…
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- Springer NatureLondon
- Administer contracts for authors and contributors and external editors and suppliers.
- Macmillan Education provides world-class content in the most relevant,…
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- MDPI UKManchester M1 5AN
- Pay rise
- Annual leave
- Employee discount
- Cycle to work scheme
- Tech scheme
- A competitive salary, including our quarterly bonus scheme, which rewards high-performing editors.
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- EVERSANALondon
- EVERSANA is searching for an Insights Writer focused on the European pharmaceutical sector to join the NAVLIN Daily News Team, part of the NAVLIN Insights team.
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- WebMDLondon W1W 8AJ
- Basic ability to read and understand clinical or scientific data.
- Work closely with Medical Science Directors, medical writers, copy editors, creative teams,…
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View similar jobs with this employerSenior Proposal Manager
Often replies in 1 dayVCLSCambridge- As such experience with Regulatory Proposals is essential.
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- Smith & NephewField Based
- Annual leave
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- AmiculumMacclesfield SK10
- Annual leave
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- Developing and delivering high-quality content within a publications workstream for a rare disease account that is highly significant for Amiculum (project…
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- OAE Publishing Inc.Remote
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Job Post Details
Job details
Job type
- Full-time
Location
Full job description
Job Description
Medical Writer
Department: Scientific Services
Location: London
About Us
At NexGen and MedComms Experts, we believe our transformational role in communicating scientific progress has the power to shape clinical practice and improve lives.
We stand apart through strategic and creative thinking, excellence in execution, and a people-first, collaborative mindset. We partner with clients who share our ambition to challenge convention and co-create innovative solutions that make complex science accessible, engaging, and memorable.
By combining scientific depth with human-centered storytelling and digital innovation, we help medical and scientific leaders communicate with clarity, authenticity, and measurable impact.
Role Overview
Develops and delivers scientifically accurate content across a range of projects. Continues to develop writing skills, maintains TA knowledge, participates fully in client meetings and liaises with KOLs with senior support.
Responsibilities
Development & delivery of high-quality content
- Develop and deliver scientifically accurate content across a range of projects.
- Ensure consistent style across multiple projects for a single client (input into style guides).
- Take responsibility for quality of own work before review.
Knowledge of therapy areas
- Develop and maintain knowledge of relevant therapy areas — products, competitors, key trial data, terminology.
- Develop in-depth knowledge of TA, market, audiences and key messages; input into strategic communications plans (with manager guidance).
- Stay current on industry practices and regulatory developments affecting writing.
Working with internal teams, clients and KOLs
- Participate fully in client meetings to discuss scientific and editorial aspects.
- Liaise with and brief KOLs as required, with senior support.
- Act as a point of contact for clients and KOLs on specified projects.
- Collaborate with the Client Partnerships team to align scientific content to the account strategy.
Interpretation & incorporation of amendments
- Accurately interpret and incorporate review comments.
Communication & proactivity
- Manage own workload proactively; communicate clearly with internal and client teams.
- Brief, review and feed back on freelance writers; integrate freelancers into account teams.
Adherence to SOPs, laws & guidelines
- Work in alignment with agency/client processes for legal/regulatory compliance; manage upload and referencing for review.
- Adhere to compliance laws, guidelines and agency/client SOPs.
- Following training, work in alignment with processes (agency and/or client) for legal/regulatory compliance (ABPI, EFPIA, FDA, PAAB, IMC codes); upload and reference items for review.
Congress / meeting support
- Attend congresses, advisory boards, or client meetings to provide writing or client support; debrief team afterwards.
Business development
- Work with manager on pitches and proposals — unmet needs research, ideas and recommendations.
- Propose new ideas for organic growth.
Financial awareness
- Full understanding of project budgets; collaborate with team to ensure efficient working.
- Complete timesheets daily.
Qualifications & Experience
- Degree level or higher in a biomedical science.
- 1–2 years’ med comms agency experience with strong evidence of teamwork.
- Desirable: PhD, MD, PharmD.
Core Competencies
- Excellent attention to detail; good grammar and syntax.
- Strong project management and organizational skills; some understanding of commercial drivers.
- Excellent interpersonal and communication skills; works well in a team under pressure.
- Excellent use of MS PowerPoint and Word.
- Solid understanding of drug development and EU/US regulations.
- Top-quality scientific writing; adapts content/style for different audiences.
- Conducts thorough literature searches and appraises results.
What Success Looks Like
- Consistently delivers high-quality projects on time and to budget.
- Adheres to compliance laws, guidelines and SOPs.
- Drives clear, proactive communication across the account team.
- Liaises confidently with KOLs and clients on specified projects.
- Achieves billability target of 80% live/active projects.
This job description is intended to outline the general nature and key responsibilities of the role. It is not an exhaustive list, and duties may evolve over time.
Why Join Us
We believe our role in communicating scientific progress has the power to shape clinical practice and improve lives. Our teams combine strategic and creative thinking, scientific depth, and digital innovation to make complex science accessible, engaging, and actionable.
You’ll be joining a company built on a strong foundation of excellence and collaboration — one that’s now scaling globally to redefine what partnership, purpose, and performance mean in medical communications. As we enter our next phase of growth, we’re expanding our reach, evolving our offerings, and building on the success of our founders and teams to become the destination agency that everyone wants to work for, work with, and be supported by.
We are an equal opportunity employer committed to fostering a diverse and inclusive workplace.