Medical Editor Job at Oxford PharmaGenesis (Cardiff, Oxford)

Editor

Become a central figure for the editorial success of EMJ, AMJ, and EMJ Learning....

Location

United Kingdom , London

Salary:

70000.00 - 75000.00 GBP / Year

EMJ

Expiration Date

Until further notice

Requirements

6+ years of experience at manager level in medical or healthcare publishing
Experience in coaching and developing an editorial team of eight or more
High standards for quality and ethics
Diligent about monitoring journal standards and ensuring compliance with regulations like ABPI
Forward-thinking, keeping up to date with the latest medical innovations
Exceptional at leading SEO best practices
Confident communicator who can share insights, learnings, and challenges with a management team
Hold a medical science-related degree (is preferred)

Job Responsibility

Lead and Mentor the Editorial Team
Ensure Gold-Standard Quality & Compliance
Strategise and Innovate Content
Drive Brand Expansion
Elevate Digital Presence
Contribute to Company Management

What we offer

Bupa medical cashback after probation
Aviva private medical insurance after one year
25 days of holiday, plus an extra day for each year of service up to 30 days
Enhanced maternity leave
Bike to Work scheme
Summer Ball
Festive Christmas celebrations
Company-wide events

Fulltime

Medical Writer

The Medical Writer applies basic to intermediate documentation preparation and d...

Location

United Kingdom , London

Salary:

Not provided

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Bachelor’s or higher degree preferred
scientific focus desirable
University-level medical or technical writing course(s) or equivalent experience in science/technical writing
Evidence of medical writing career development desirable, eg, American Medical Writers Association certificate, Editor in Life Sciences certificate, or relevant training through Drug Information Association
Up to 2 years as a medical writer in the pharmaceutical industry or at least 5 years of medical or scientific writing experience as a primary job responsibility
Familiar with drug development process (discovery to market)
Basic understanding of biostatistical and clinical research concepts
Basic applied knowledge of documentation required for the conduct of clinical studies, protocol design, study results reporting
Writing high-quality documents that support corporate goals and objectives
Experience writing, reviewing, or editing protocols and clinical study reports preferred

Job Responsibility

Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PBRERs, DSURs, etc.)
Aids in managing study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
Adheres to departmental procedures and practices and technical and industry standards during all aspects of work
Assists in developing and reviewing standard processes and templates within Global Medical Writing
Works effectively with cross-functional groups within BioMarin
Other tasks as assigned

Fulltime

Medical Writer

The Medical Writer 1 applies basic to intermediate documentation preparation and...

Location

United States , San Rafael

Salary:

74100.00 - 100000.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Bachelor’s or higher degree preferred
scientific focus desirable
University-level medical or technical writing course(s) or equivalent experience in science/technical writing
Evidence of medical writing career development desirable, eg, American Medical Writers Association certificate, Editor in Life Sciences certificate, or relevant training through Drug Information Association
Up to 2 years as a medical writer in the pharmaceutical industry OR At least 5 years of medical or scientific writing experience as a primary job responsibility
Familiar with drug development process (discovery to market)
Basic understanding of biostatistical and clinical research concepts
Basic applied knowledge of documentation required for the conduct of clinical studies
Basic applied knowledge of protocol design
Basic applied knowledge of study results reporting

Job Responsibility

Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PBRERs, DSURs, etc.)
Aids in managing study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
Adheres to departmental procedures and practices and technical and industry standards during all aspects of work
Assists in developing and reviewing standard processes and templates within Global Medical Writing
Works effectively with cross-functional groups within BioMarin
Other tasks as assigned

What we offer

discretionary annual bonus
discretionary stock-based long-term incentives
paid time off
company-sponsored medical, dental, vision, and life insurance plans

Fulltime

New

Senior Medical Writer

The Senior Medical Writer applies advanced documentation preparation and documen...

Location

United States

Salary:

142100.00 - 159500.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Up to 6 years of as a medical writer in the pharmaceutical industry – OR - at least 10 years of medical or scientific writing experience as a primary job responsibility
Experience writing, reviewing, or editing protocols and clinical study reports required
Experience writing, reviewing, or editing INDs, BLA/NDAs, PBRERs, DSURs, and PAERs highly preferred
Experience writing, reviewing, or editing regulatory briefing books preferred
Advanced applied knowledge of routine document content preparation, including the use of style guides (internal, AMA, CBE, Chicago), medical dictionaries, and guidance documents that prescribe content
Ability to interpret and create complex tabular and graphical clinical data presentations
Advanced applied knowledge of basic clinical laboratory tests
Understanding of the concepts of coding dictionaries (MedDRA, WHO Drug)
Advanced understanding of the drug development process (discovery to market), biostatistical and clinical research concepts, clinical study conduct, clinical study data collection, database management, data integration, and generation of datasets
Intermediate to advanced understanding of scientific concepts integral to nonclinical development, CMC, PK, PD, and antibody detection

Job Responsibility

Applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications
Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PBRERs, DSURs, etc.)
Drafts and edits documents used in the preparation of regulatory filings (eg, briefing books, eCTD Module 2/Module 5 clinical or integrated summaries)
Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
Represents Global Medical Writing at cross-functional team meetings (eg, study team, development team, other subteams)
Builds effective partnerships with cross-functional groups to ensure customer/stakeholder needs are met
Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
Assists in developing and reviewing standard processes and templates within Global Medical Writing, and may also review/consult on the development of standard processes and templates in other departments
Adheres to departmental procedures and practices and technical and industry standards during all aspects of work

What we offer

Discretionary annual bonus
Discretionary stock-based long-term incentives (eligibility may vary based on role)
Paid time off
Company-sponsored medical, dental, vision, and life insurance plans

Fulltime

Senior Medical Writer

The Senior Medical Writer applies advanced documentation preparation and documen...

Location

United States , San Rafael

Salary:

116000.00 - 159500.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Up to 6 years of as a medical writer in the pharmaceutical industry – OR - at least 10 years of medical or scientific writing experience as a primary job responsibility
Experience writing, reviewing, or editing protocols and clinical study reports required
Experience writing, reviewing, or editing INDs, BLA/NDAs, PBRERs, DSURs, and PAERs highly preferred
Experience writing, reviewing, or editing regulatory briefing books preferred
Advanced applied knowledge of routine document content preparation, including the use of style guides (internal, AMA, CBE, Chicago), medical dictionaries, and guidance documents that prescribe content
Ability to interpret and create complex tabular and graphical clinical data presentations
Advanced applied knowledge of basic clinical laboratory tests
Understanding of the concepts of coding dictionaries (MedDRA, WHO Drug)
Advanced understanding of the drug development process (discovery to market), biostatistical and clinical research concepts, clinical study conduct, clinical study data collection, database management, data integration, and generation of datasets
Intermediate to advanced understanding of scientific concepts integral to nonclinical development, CMC, PK, PD, and antibody detection

Job Responsibility

Applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications
Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PBRERs, DSURs, etc.)
Drafts and edits documents used in the preparation of regulatory filings (eg, briefing books, eCTD Module 2/Module 5 clinical or integrated summaries)
Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
Represents Global Medical Writing at cross-functional team meetings (eg, study team, development team, other subteams)
Builds effective partnerships with cross-functional groups to ensure customer/stakeholder needs are met
Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
Assists in developing and reviewing standard processes and templates within Global Medical Writing, and may also review/consult on the development of standard processes and templates in other departments
Adheres to departmental procedures and practices and technical and industry standards during all aspects of work

What we offer

Discretionary annual bonus
Discretionary stock-based long-term incentives
Paid time off
Company-sponsored medical, dental, vision, and life insurance plans

Fulltime

Assistant Editor - Medical Sciences

Kick-start your career in academic publishing: join MDPI in Basel as an Assistan...

Location

Switzerland , Basel

Salary:

Not provided

MDPI

Expiration Date

Until further notice

Requirements

Master’s or PhD degree in one of the following fields: Medicine, Clinical Sciences, Pharmacy, Biomedical Sciences, or related health- and life-science fields
Excellent written and spoken English skills
Advanced knowledge of MS Office applications (Word, Excel, PowerPoint)
Passion for scientific research and academic publishing
Team player with the capability to work in a dynamic, international environment
Detail-oriented with the capacity to see the big picture
Strong organizational and time management skills
Very good communication and coordination skills

Job Responsibility

Support the editorial process for academic research journals in your domain of expertise
Organize the peer review process for submitted manuscripts and coordinate editorial decisions
Be in charge of formatting manuscripts according to our in-house standards
Handle email communication between all parties involved in the publication process
Ensure that scholarly articles are accurately edited and published with a high degree of consistency and within the deadlines
Serve as key point of contact between the Editorial Office and external authors and readers

What we offer

Flexible working hours
Team bond strengthening through team-building events
Professional growth opportunities with our global training system
Working in a collaborative, diverse, and socially responsible team
Company retreat facility
Full-coverage insurance for accidents/daily sickness
Prime location near Basel train station and city center

Fulltime

Managing Editor

Bring your expertise to EMJ and create content that informs, engages, and makes ...

Location

United Kingdom , London

Salary:

55000.00 GBP / Year

EMJ

Expiration Date

Until further notice

Requirements

hands-on experience in scientific or medical publishing or communications, with a strong understanding of compliance, ethical standards, and industry regulations
experience in managing and executing peer review processes, ensuring content accuracy, credibility, and integrity
3+ years of line-management experience, guiding and developing team members to deliver high-quality work

Job Responsibility

Oversee peer review: Manage the peer review process, resolve queries, and ensure content quality and target delivery
Maintain processes and compliance: Keep editorial and commercial procedures updated, efficient, and aligned with industry standards
Manage the publishing schedule: Develop and maintain the Editorial Publishing Schedule with the Editor, ensuring timely content delivery
Deliver KPIs and reporting: Own departmental KPIs and produce performance reports for journals and staff
Lead team performance: Guide staff development, oversee team performance, and line-manage Associate Editors
Promote wellbeing and progression: Monitor team wellbeing and support motivation and career growth
Strengthen cross-team collaboration: Foster strong communication and working relationships between Editorial and Commercial teams
Support team training: Coordinate and deliver training for new and existing team members
Contribute to editorial strategy: Work with the Editor to shape content themes and support strategic direction

What we offer

Bupa medical cashback after probation
Aviva private medical insurance after one year
25 days of holiday, plus an extra day for each year of service, up to 30 days
enhanced maternity leave
Bike to Work scheme
Summer Ball
festive Christmas celebrations
company-wide events

Fulltime

Copy Editor

This is an opportunity to work for international clients from our Uruguay office...

Location

Uruguay , Montevideo

Salary:

Not provided

Hogarth

Expiration Date

Until further notice

Requirements

Have an understanding of advertising, communication, and business processes
Conduct research and read medical content
Be confident working with a multi-disciplinary team in a production environment
Have an excellent command of the English language both verbal and written
Be comfortable working with international clients
Work under pressure to meet tight deadlines
Full-time onsite availability during the first three months (from 09:30 to 19:00hr)
Verifiable experience working on the role
Experience with pharma, medical, or scientific content, translation, proofreading, creating content or copy editing

Job Responsibility

Proofreading heavy content, amending grammatical, spelling, and punctuation errors, as well as making sure the copy follows the proper brand style guidelines
Create, review and approve client assets for various channels and marketing platforms using predefined pharma industry and brand guidelines and guardrails
Responsible for proofreading and content quality
Editing and reviewing content for correctness, creating creative briefs, and approving assets

What we offer

Hybrid working model
Collaborative, borderless environment
Access to diverse projects, global career opportunities
Inclusion and Impact
Fostering a culture of respect

Fulltime

Medical Editor

Oxford PharmaGenesis

Location:
United Kingdom , Cardiff, Oxford

Category:
Media

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 10, 2026

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