Clinical Editor jobs
- VeristatUnited Kingdom
- Ability to lead submission-level sections (clinical documents, e.g., Clinical Study Reports, Protocols, Investigator Brochures, Integrated Summary of Safety and…
View similar jobs with this employerInizio EvokeLondon- Company pension
- Cycle to work scheme
- Translate complex scientific and clinical data into accessible messaging that aligns with brand strategy and regulatory requirements.
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- Haymarket Media GroupLondon TW1 3SP
- Company pension
- Paid volunteer time
- Flexible schedule
- The MIMS Healthcare Network encompasses a portfolio of trusted, well-established brands including GPonline, GP Business, MIMS and MIMS Learning, designed to…
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- Haymarket Media GroupLondon TW1 3SP
- Company pension
- Paid volunteer time
- Flexible schedule
- The MIMS Healthcare Network encompasses a portfolio of trusted, well-established brands including GPonline, GP Business, MIMS and MIMS Learning, designed to…
- View all Haymarket Media Group jobs - London jobs
- Salary Search: Associate Editor salaries in London
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View similar jobs with this employerPublic Library of ScienceCambridge- Company pension
- Paid volunteer time
- Private medical insurance
- The Associate Editor oversees the editorial process for manuscripts submitted to PLOS journals.
- This role will require the use of prior research experience,…
- WileyRemote
- Wiley’s Advanced journal portfolio is looking for a dynamic and ambitious individual to join the team as Editor-in-Chief (Advanced Fabrication).
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Medical Education Content & Programme Coordinator (Doctor)
NewOften replies in 1 dayBromley Emergency Training & Research LtdLondon SE1- Discounted or free food
- The postholder will coordinate clinical content contributors and senior reviewers, undertake appropriate initial clinical and editorial review, maintain an…
- Thermo Fisher ScientificRemote
- Write and edit clinical and regulatory documents, including clinical study reports, protocols, investigator brochures, and regulatory submissions.
View similar jobs with this employerThermo Fisher ScientificRemote- Duties could include researching, writing and editing clinical study reports and protocols, summarizing data from clinical studies, writing or providing input…
View similar jobs with this employerThermo Fisher ScientificRemote- You will be an established Medical Writing leader with extensive experience gained within clinical research, the pharmaceutical/biotechnology industry, a CRO or…
View similar jobs with this employerThermo Fisher ScientificRemote- Researches, writes, and edits clinical study reports and study protocols, and summarizes data from clinical studies.
- EmotiveLondon W1B 1NT
- Annual leave
- Sabbatical
- Gym membership
- Company pension
- Private medical insurance
- You'll also have the opportunity to work on creative projects, collaborating with scientific, account and creative teams to develop engaging campaigns and…
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- Ogilvy Health UKLondon
- You will be the scientific anchor on key publications, taking ownership of clinical study manuscripts from inception to submission.
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- WileyOxford
- Wiley's Comprehensive Editorial Evaluation Team (CEET), responsible for managing the peer-review process and decision-making for a portfolio of >120 in-house…
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- Hearst Media ServicesLondon SW1Y 4AJ
- Employee discount
- Company pension
- Paid volunteer time
- Discounted gym membership
- Cycle to work scheme
- Season ticket loan
- Work closely with the Multiplatform Director (MD) to optimise workflow, allowing writers and editors to contribute to all the brand’s platforms while achieving…
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- Springer NatureLondon
- In this role you will be play a critical role in ensuring a high‑quality, efficient, and integrity‑driven peer review process for journals within the Computer…
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Job Post Details
Principal Medical Writer- Clinical Focus - job post
Job details
Job type
- Full-time
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.