Senior medical writer Jobs

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

New

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

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 Copywriter

Robert Half has a client seeking a Senior Copywriter with a pharmaceutical adver...

Location

United States , Villanova

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Professional experience working in the pharmaceutical advertising space
Extensive experience writing for HCP audiences, specifically in the Oncology sector
Comfortability with the freelance work model and fluctuating work hours

Job Responsibility

Craft clear, engaging, and accurate copy for a variety of materials, including clinical brochures, white papers, patient resources, sales aids, email campaigns, websites, product profiles, and presentations targeting healthcare professionals
Translate complex oncology-related scientific data into precise, digestible messaging for HCPs while adhering to regulatory compliance and medical accuracy
Partner with creative teams, medical writers, account managers, and client stakeholders to develop targeted campaigns that align with brand strategies

What we offer

Medical, vision, dental, and life and disability insurance
Eligibility to enroll in 401(k) plan
Access to free online training

Parttime

Associate Creative Director, Copy

We are looking for an Associate Creative Director (Copy) who is a master of lang...

Location

United States , Cary; New York; Philadelphia

Salary:

125000.00 - 175000.00 USD / Year

Inizio Evoke

Expiration Date

Until further notice

Requirements

Master of language, storytelling, and strategic communication
Passionate about translating complex scientific and medical information into compelling narratives
Excel at developing writers to deliver impactful, high-quality content
Proven ability to craft impactful and compliant messaging across multiple channels
Inspiring leader and mentor, passionate about fostering talent and guiding teams
Strategic thinker, who understands how copy influences brand positioning, engagement, and behavior change
Highly skilled in adapting tone and voice, writing across various audiences, including healthcare professionals, patients, and caregivers
Meticulous editor, ensuring clarity, accuracy, and alignment with regulatory and brand guidelines
Collaborative partner, who enjoys working with designers, strategists, and account leads
Continuous learner, staying updated on industry trends, regulations, and best practices

Job Responsibility

Be the brand voice expert, ensuring consistency and effectiveness across all written materials
Mentor a team of Copywriters and Senior Copywriters, developing their writing skills and strategic thinking
Create and refine messaging strategies, creating compelling and approvable copy that aligns with brand positioning and market insights
Collaborate closely with Art, Strategy, and Medical teams, integrating copy seamlessly with visual storytelling
Oversee the development of messaging platforms, ensuring consistency across digital, print, social, and video
Navigate and apply regulatory requirements, ensuring all copy is compliant while maintaining creative excellence
Present and defend creative work to clients, regulatory teams, and internal stakeholders
Stay ahead of industry trends, continuously evolving brand messaging to remain relevant and engaging

What we offer

Fully remote work environment
Competitive compensation
Company-paid medical
Company-paid dental
401(k)
Tuition reimbursement
Flexible time off

Senior Director, Clinical and Regulatory Writing

The Senior Director, Clinical and Regulatory Writing will serve as a strategic l...

Location

United States , Philadelphia

Salary:

Not provided

Cabaletta Bio Inc

Expiration Date

Until further notice

Requirements

Advanced degree in life sciences (M.D., or PharmD preferred)
MS, PhD with significant clinical pharmacology writing experience will be considered
12+ years of progressive experience in regulatory or scientific/medical writing in the biopharmaceutical industry, including 5+ years in a leadership role
Demonstrated experience developing content for major global regulatory submissions (e.g., IND, BLA, MAA), preferably in cell or gene therapy
Strong understanding of drug development processes, regulatory frameworks (FDA, EMA, ICH), and clinical trial documentation requirements
Exceptional writing, editing, and analytical skills with the ability to convey complex scientific data clearly and persuasively
Proven leadership capabilities, including team development, cross-functional collaboration, and vendor management
Proficiency in Microsoft Office Suite, document management systems (e.g., Veeva Vault), and electronic publishing tools
Strong project management skills with the ability to prioritize competing demands in a fast-paced, deadline-driven environment
Collaborative mindset with the ability to influence and guide stakeholders across disciplines and levels of seniority

Job Responsibility

Lead the clinical writing function in the development, review, and approval of regulatory documents to support global submissions (e.g., INDs, IMPDs, BLAs, MAAs, Orphan Drug Applications, Investigator Brochures, protocols, clinical study documents, PSPS/POIPs, Prime, RMAT)
Lead cross-functional content planning of regulatory submission modules, including data integration and interpretation, and ensuring consistency in strategic messaging for dossiers, meeting packages and responses to health authorities
Translate complex technical data from clinical and biostatistics teams into scientifically accurate, submission-ready documentation
Manage external consultants and contractors as needed to support Cabaletta submissions reviews, authoring, if needed, and gap analyses
Mentor, train, and manage a team of medical/regulatory/technical writers or cross-functional contributors in document development
Develop and implement strategic plans for medical writing activities, aligning them with clinical development, regulatory affairs, and overall business goals
Drive process improvements and develop standard practices for efficient, compliant and high-quality document delivery
Collaborate with Clinical Operations and external CROs to ensure inspection readiness of clinical trial documentation, including informed consents, study manuals, and IRB/IBC responses

What we offer

health and retirement, PTO, and stock option plans

New

Associate Vice President of Workforce, Innovation, and Strategic Partnerships

The Associate Vice President (AVP) of Workforce, Innovation and Strategic Partne...

Location

United States , Hughesville

Salary:

Not provided

Beatrice Daily Sun

Expiration Date

Until further notice

Requirements

Bachelor's degree with 10 years of experience working in industry, or in education, workforce development, business, public administration or related fields
Minimum of five (5) years of progressive leadership experience in workforce development, continuing education, industry or related fields
Demonstrated success in partnership development with business, government and community organizations
Proven ability to lead complex projects, manage budgets, and supervise cross-functional teams
Demonstrated excellence in oral, written, and interpersonal communication skills, with the ability to interact effectively with diverse populations
Proven ability to work independently, manage time effectively, and prioritize multiple tasks in a dynamic environment
Adaptable and responsive to a fast-paced and evolving work setting, with the capacity to manage change constructively
Knowledge of adult and community education with experience in the development and delivery of educational programming
Proficient in the use of integrated data systems, with the ability to interpret and apply technical information accurately
Skilled in the use of Microsoft Office Suite, educational technologies, and standard office equipment to support program operations

Job Responsibility

Provide visionary strategic leadership in the planning, development and delivery of non-credit and credit-aligned workforce programs
Serve as the internal lead/champion the development of high-impact career pathways that include stackable credentials, registered apprenticeships, industry certifications, and seamless transfer options
Lead cross-functional teams to implement high-demand workforce pathways
Identify emerging workforce trends and proactively guide program design
Partner on the design and expansion of dual enrollment and early college experiences that connect high school students to workforce-aligned career and technical education (CTE) pathways
Proactively analyze national and global workforce trends to provide detailed summaries and analysis
Advance initiatives that embed innovation in workforce program delivery
Lead efforts to integrate emerging innovations into program design and delivery
Develop and scale bold strategies to scale workforce access for underserved, rural, underemployed and other targeted populations
Foster and maintain cross-departmental and division collaboration

What we offer

Excellent health insurance benefits
State Retirement Pension plan
wellness programs
Code Green early closure Fridays in the summer
college closure for spring break and several major holidays, including the week between Christmas and New Year
and for several days in March for Spring Break

Fulltime

Senior medical writer

Randstad

Location:
India , Bengaluru

Category:
Media

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
December 23, 2025

Expiration:
February 16, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Senior medical writer

Senior Healthcare Content Writer

Senior Content Manager

Regulatory Writing Senior Manager

Senior Physician, Patient Safety

Senior Copywriter

Associate Creative Director, Copy

Senior Director, Clinical and Regulatory Writing

Associate Vice President of Workforce, Innovation, and Strategic Partnerships

Senior medical writer

Randstad

Location:India , Bengaluru

Category:Media

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:December 23, 2025

Expiration:February 16, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Senior medical writer

Senior Healthcare Content Writer

Senior Content Manager

Regulatory Writing Senior Manager

Senior Physician, Patient Safety

Senior Copywriter

Associate Creative Director, Copy

Senior Director, Clinical and Regulatory Writing

Associate Vice President of Workforce, Innovation, and Strategic Partnerships

Location:
India , Bengaluru

Category:
Media

Contract Type:
Not provided

Job Posted:
December 23, 2025

Expiration:
February 16, 2026