Senior Medical Writer Job at Oxford PharmaGenesis (Oxford)

Senior medical writer

Medical Communication Writer to lead content development across scientific, bran...

Location

India , Bengaluru

Salary:

Not provided

Randstad

Expiration Date

February 16, 2026

Requirements

Master’s degree or higher in Life Sciences, Medicine, Pharmacology, or a related field
Minimum 3-5 years’ experience in scientific writing, content development, or medical communications
Proven experience working with branded pharma content and omnichannel communication assets
Demonstrated skill in simplifying complex science for patients and general audiences
Experience managing junior writers and reviewing their content

Job Responsibility

Draft, review, and edit high-quality content: research summaries, visual aids, video scripts, IVAs, brochures, web copy, etc.
Interpret complex clinical/scientific data and translate into HCP, patient, and consumer-friendly formats
Align content with brand strategy and therapeutic positioning for branded and non-branded campaigns
Lead content planning across omnichannel pharma journeys
Collaborate with creative, data, and development teams to ensure integrated delivery
Participate in client discussions and strategy meetings
guide junior writers with reviews and training
Ensure scientific accuracy, regulatory compliance, and consistency across all deliverables

Senior Healthcare Content Writer

Our client, a leader in the healthcare insurance space, is seeking a highly skil...

Location

United States , Atlanta

Salary:

Not provided

Tier4 Group

Expiration Date

Until further notice

Requirements

A Bachelor’s degree, preferably in English, Journalism, Marketing or communications
Minimum of 7-10 years’ experience
Corporate experience with the ability to interact with C-level executives
Superior creative and technical writing and grammar skills
Experience in medical or healthcare communications and writing with a strong understanding of medical terminology and healthcare industry practices
Proven ability to translate complex analyses into engaging, clear, and impactful content
Understanding of SEO and writing meta data, keywords, and alt text
Knowledge of MS Office applications including Word and PowerPoint
Openness to a rapidly changing and growing environment
A self-starter that’s able to work both independently and collaboratively on multiple projects concurrently

Job Responsibility

Research and write articles, white papers, reports, presentations, courses, and other content primary for the website, but channels also could include print, video, social, email, and more
Work with analytics team to highlight liability risk and incorporate analytics insights throughout content
Edit learning content developed by medical and legal faculty
Collaborate with the Chief Medical Officer, Director, Advice Content Strategy, and subject matter experts to research and develop ideas for new content
Work closely with the marketing team to optimize copy for digital channels, including SEO
Deliver work that reflects a careful attention to detail and adherence to legal and brand guidelines

Fulltime

Senior Content Manager

Lead the development, review, and delivery of high-impact medical education cont...

Location

Canada , Toronto

Salary:

Not provided

Fullscript

Expiration Date

Until further notice

Requirements

8+ years in medical writing and editing, preferably with a focus on practitioner education
Deep understanding of scientific writing standards, editorial best practices, and regulatory requirements
Proven ability to write across modalities and tones—from protocols to presentations to podcast scripts
Confidence collaborating with freelancers and SMEs, setting expectations, and providing editorial direction
Familiarity with using AI tools to support content development, with strong human oversight

Job Responsibility

Create and oversee the development of evidence-informed educational content for healthcare professionals
Direct freelance medical writers, providing clear outlines, editorial guidance, and constructive feedback
Collaborate cross-functionally with internal teams and stakeholders to shape content formats and delivery strategies
Tailor content for diverse audiences and formats
Ensure quality and compliance by conducting or reviewing literature searches, validating accuracy of claims, reviewing for FTC/FDA compliance, and adhering to internal style and compliance guidelines
Conduct clear content intake processes to define context, audience, CME requirements, and format
Identify opportunities to improve workflows for editing, reviewing, and approving medical content
Ensure content quality and utility by measuring performance, applying insights, and adapting content to better meet user needs and maximize impact

Fulltime

Regulatory Writing Senior Manager

In this key role you will serve as the functional area lead on product teams, le...

Location

United States

Salary:

152684.00 - 193308.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 2 years of directly related experience
Master’s degree and 6 years of directly related experience
Bachelor’s degree and 8 years of directly related experience
Associate’s degree and 10 years of directly related experience
High school diploma / GED and 12 years of directly related experience
Experience with regulatory documents in Regulatory Affairs, Research, Development or related area
5+ years of experience in medical writing in the Biotech/Pharmaceutical industry

Job Responsibility

Author or oversee the authoring of all regulatory submission documents including Clinical Study Reports, Investigator Brochures, Responses to Questions, Protocols, Protocol Amendments, Informed Consent Forms, Table of All Studies, Clinical Overview Addenda, eCTD Module 2 Clinical Summary Documents, Briefing Documents, and Pediatric Investigation Plans
Conduct the formal review and approval of authored documents, following applicable standard operating procedures
With limited supervision, lead regulatory writing activities for complex product submissions, including new and supplemental drug applications/biologics license applications
Serve as functional area lead on product teams (e.g., Global Regulatory Team, Evidence Generation Team, Global Safety Team, Label Working Group)
Provide functional area input for Global Regulatory Plan and team goals
Supervise the work of contract and freelance writers and mentor junior medical writers as assigned
Lead departmental and cross-departmental initiatives, as appropriate
Generate document timelines

What we offer

Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans and bi-annual company-wide shutdowns
Flexible work models, including remote work arrangements, where possible

Fulltime

Medical Affairs Medical Writer

Medical Affairs is responsible for ensuring the safety and efficacy of Medicatio...

Location

United States , Sandy, UTAH

Salary:

39.00 - 41.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

Experience in a relevant Medical Device Industry required
Minimum of 2-3 years writing experience within the Medical Device Industry.
Superior attention to detail.
Ability to write with scientific accuracy
Ability to compile, write, edit, and format documents for submission to regulatory agencies. (Writing samples required)
Ability to assist with comprehensive literature searches as needed.
Understanding of MEDDEV 2.7/1 rev4 guidelines and the MDR regulations related to clinical evaluation reports preferred.
Ability to ensure that all deliverables are in accordance with applicable regulations, standards, and guidelines
Excellent written and verbal communication skills.
Proficiency in MS Office with expertise in Microsoft Word with a special focus on word processing, use of templates, and formatting. Working knowledge of Excel.

Job Responsibility

Combine knowledge of science with understanding of research and writing to present information effectively and with clarity.
Focus on scientific medical writing to prepare documents – clinical evaluation plans (CEPs) and clinical evaluation reports (CERs) – for submission to regulatory bodies.
Collaborate with other functions and with the Senior Medical Writer as necessary to ensure accurate and timely completion and review of clinical documents for regulatory submissions.
Assist with and / or compile, review and summarize, available data to access the safety and efficacy of MDS products worldwide.

Fulltime

New

Senior Medical Writer

The Senior Medical Writer: 1) writes original content for publications activitie...

Location

United States , West Chester

Salary:

Not provided

Synchrony Group

Expiration Date

Until further notice

Requirements

PhD, PharmD, or MD
Minimum of 3 years’ experience in medical communications
Substantial professional medical writing experience in a wide variety of communication formats
Ability to work independently on assigned projects
Excellent attention to detail and high degree of scientific and medical accuracy
Ability to manage outcomes to win-win resolution
Ability to identify key issues and to creatively and strategically overcome challenges or obstacles
High level of integrity, ethics, confidentiality, and accountability
Sound analytical thinking, planning, prioritization, and execution skills with an ability to multitask
Well-developed professional communication skills, including written and interpersonal

Job Responsibility

Demonstrate a command of assigned therapeutic areas and expertise with assigned products
Write original content for publication/communication activities (primary and review manuscripts, abstracts, posters), slide presentations, meeting summaries, and other materials for HCP and internal audiences
Prepare materials according to internal writing guidelines and other applicable guidelines (eg, client-specific style guidelines, compliance best practices, journal style guidelines)
Follow all internal processes and procedures with regard to workflow, development of deliverables, and adherence to industry best practices, including GPP3
Demonstrate the flexibility/adaptability necessary to function on different therapeutic teams as needed
Interpret and apply clinical data
Maintain a proactive approach on initiatives for existing and prospective clients
Work in conjunction with team members to manage workload and develop and adhere to logical and attainable timelines for project completion
Attend team meetings to provide input and aid in troubleshooting/problem-solving
Efficiently and accurately collate and incorporate author/client comments

What we offer

Competitive salaries
Generous paid time off
Excellent health insurance
Family leave
401(k) plan with employer matching

Fulltime

New

Senior Medical Writer - FSP

As a Medical Writer at Parexel, your strong scientific knowledge, writing skills...

Location

United States

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Bachelor's degree in Life Sciences/Health Related Sciences or equivalent
Demonstrated understanding of clinical research, the drug development process, and industry guidelines and regulations, e.g., ICH-GCP
Extensive clinical/scientific writing skills
Scientific background essential
writing experience includes multiple clinical documents: study reports, study protocols, or CTD documents or similar
Advanced word processing skills, including MS Office (expertise in Word)
software and systems knowledge or ability to learn and adapt to various IT systems: document management systems, collaborative authoring (e.g., SharePoint), and file conversion and databases (Excel)
Fluent in written and spoken English with appropriate attention to phraseology, grammar, and punctuation
Excellent interpersonal, verbal, and written communication skills
Ability to consistently produce documents of high quality

Job Responsibility

Author Clinical Documents: Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports, and integrated summaries of safety and efficacy
Revise document drafts based on the review comments from team members to ensure inclusion of all relevant input
Follow required standard operating procedures (SOPs), templates, guidelines, regulations, client instructions and other processes, as applicable
Perform literature searches/reviews as necessary to obtain background information and training for development of documents
Review statistical analysis plans and mock statistical output to determine appropriateness of content/format for clinical writing
Quality Control: Ensure that all work is complete and of high quality prior to team distribution or shipment to client
Confirm data consistency and integrity across the document
Prepare documents for publishing readiness, when applicable
Ensure document structure, content, and style adheres to FDA/EMA or other appropriate regulatory guidelines, and comply with departmental, corporate or client SOPs and style guidelines, as applicable
Provide suggested alternative content when contributors provide content that does not meet document needs

What we offer

Foster a culture of inclusivity, collaboration, and support
Continuous learning from being mentored to job shadowing, job rotation, and stretch assignments, as well as becoming a mentor or leading a team
Development and promotion based on global standards and your personal development plan
Supportive and inclusive environment
Career growth and development
Mentorship
Flexible work
Diverse projects
Culture of excellence
Global exposure

Senior Physician, Patient Safety

Join our dynamic Patient Safety team as a Senior Physician where you'll leverage...

Location

United States; Canada , Remote; Alberta

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Experience in clinical medicine (general or specialist qualifications) which is expected to be kept up to date
Good knowledge of drug safety and the drug development process
Good knowledge/understanding of medical terminology
Relevant experience in pharmacovigilance/ Drug Safety/ Clinical Practice
3 - 5 years previous experience in pharmacovigilance and/or medical monitoring is required
US Board Certification/board eligibility or regional equivalent for Canada
Bachelor of Medicine, Bachelor of Surgery (MBBS) / Doctor of Medicine (MD)/ Medically qualified from an acknowledged Medical School
Completion of at least basic training in clinical medicine (residency, internship etc.)
Demonstrated success in technical proficiency and scientific creativity
Good presentation and verbal/written communication skills

Job Responsibility

Maintaining a good working knowledge of the Adverse event/Safety profile of assigned products, labeling documents, data handling conventions, client’s guidelines and procedures, and global drug safety regulations and guidelines
Maintaining an awareness of global regulatory requirements, reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting
Performing medical review of cases not limited to (including complex and challenging cases requiring expert judgement)), clinical trial, and literature cases including combination products {drug-device}) according to client/Parexel Standard Operating Procedures (SOPs
as applicable) and liaising with the client, as require
Writing Pharmacovigilance/Marketing Authorization Holder (MAH) comment and assessing company causality
Review appropriateness of medical content in narrative for medical coherence
Assessing seriousness, listedness / expectedness of reported events
Providing medical inputs to case processing team
Raising appropriate follow-up queries for relevant information from the reporter/HCP (Health Care Professional)
Review and verify appropriate selection of adverse events from source documents, assign appropriate Medical Dictionary for Regulatory Activities (MedDRA) code, review narrative

What we offer

Flexible approach to work that meets your personal needs
Work from home
Benefits vary by country
Investment in your professional and personal development

Senior Medical Writer

Oxford PharmaGenesis

Location:
United Kingdom , Oxford

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 10, 2026

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