Medical Writing Trainee jobs
- VeristatUnited Kingdom
- Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting.
- MDPI UKManchester M1 5AN
- The position of Assistant Editor is an entry-level, full-time and permanent position based in our city centre office in Manchester, UK.
- Kinetix Health GroupLondon W1W
- Stay current on industry practices and regulatory developments affecting writing.
- Top-quality scientific writing; adapts content/style for different audiences.
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- ClarioRemote
- Contribute to process improvements and best practices within scientific and medical writing activities.
- Minimum 5 years' experience in medical, scientific or…
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- WebMDLondon W1W 8AJ
- This role is well suited for someone early in their medical communications career who is eager to build strong editorial and scientific skills while working on…
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View similar jobs with this employerThermo Fisher ScientificRemote- Experience in managing and directing complex medical writing projects required.
- May serve as backup medical writer.
- Thermo Fisher ScientificRemote
- Experience in managing and directing complex medical writing projects required.
- Excellent data interpretation and medical writing skills, including grammatical,…
- Thermo Fisher ScientificRemote
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- サイネオス・ヘルスMO
- Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal…
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- Axon CommunicationsToronto
- AXON is seeking an experienced medical communications professional who combines exceptional scientific writing skills with strategic thinking and a passion for…
- AcumetisLondon EC1R 3AW
- Champion best practices in medical writing, publication standards, and scientific communication.
- Review and approve evidence-generation, literature review, and…
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- IPG HealthLondonBasic Information Location GBR London 16 Old Bailey Posted Date 13-May-2026 Agency McCann Health London Department Creative Job Number 61614 Job Type Regular…
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- Proven ability to develop accurate, insightful, and compelling content across publications and other materials, with at least 3 years’ experience in medical…
View similar jobs with this employerAshfield MedCommsManchester- Several years experience in medical writing, within a medical communications agency.
- Excellent scientific writing, editing and critical appraisal skills.
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View similar jobs with this employerAshfield MedCommsManchester- Several years experience in medical writing, within a medical communications agency.
- Excellent scientific writing, editing and critical appraisal skills.
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- Red NucleusRemote
- Understanding of the AMA writing style.
- Prior experience writing peer-reviewed publications, congress abstracts, posters, and slide decks.
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Principal Medical Writer- Clinical Focus
Job details
Full job description
Job Description:
Key Purpose:
The Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with International Council for Harmonisation (ICH) and other regulatory guidelines, and individual company document standards. The Principal Medical Writer works under the direction of Medical Writing management and collaborates with cross-functional internal and external document production teams.
- 105+ approved therapies for marketing applications prepared by Veristat
- 480+ oncology projects in the past 5 years
- 350+ rare disease projects delivered in the past 5 years
- Flexible, inclusive culture — 70% remote workforce, 66% women-led teams
Experience & Minimum Requirements:
- Bachelor’s degree required; science-related field preferred.
- Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute toward this minimum requirement, as determined on a case-by-case basis.
- Ability to lead submission-level sections (clinical documents, e.g., Clinical Study Reports, Protocols, Investigator Brochures, Integrated Summary of Safety and Integrated Summary of Effectiveness) taking responsibility for clarity of purpose, leading others toward the common goal within timeline and budget on complex projects.
- Possesses broad experience and technical expertise across more than one therapy area and integrate this knowledge to deliver business successes and actively transfer this knowledge to strengthen the skill base across the organization.
- Advanced knowledge of ICH and related regulatory guidelines.
- Excellent written English and keen attention to detail.
- Strong interpersonal and communication skills.
- Experience with Microsoft Office Suite is essential, including advanced Microsoft Word proficiency.
Additional Requirements:
- Driving/Travel requirements – 0-10% (national and international)
- Physical requirements – ability to occasionally lift/move up to 25 lbs
- Hours/Conditions – minimum weekly work hours set in accordance with local regulations
- Fair Labor Standards Act Classification – Exempt
Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.
Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.