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Junior Medical Writing Jobs (NOW HIRING)

Stryker

Senior Staff Medical Writer (Remote)

Seattle, WA · On-site +1

$143K - $238K/yr

Drive continuous improvement initiatives, maintain medical writing tools and templates, and mentor junior medical writing team members. What You Need Required * Bachelor's degree in a scientific ...

New

twentysix

Medical Writer

Manhattan, NY · On-site

$65 - $110/hr

Adapts writing style to suit different audiences (e.g. primary and secondary care physicians ... Trains/mentors junior writers on writing and company processes Qualifications and skills * You ...

New

MJH Life Sciences

Principal Medical Writer

Cranbury, NJ · On-site

$95K - $105K/yr

This will require supplying accurate precise directives for each assignment, review and guidance in best practices of writing/editing, * Provide training and mentorship to junior Medical Writers and ...

Biogen, Inc.

$191 - $263/hr

## Director, Medical Writing - WCHApplyremote type: Off Campuslocations: Remote, USAtime type: Full ... Mentor and provide professional development guidance to junior writers. May serve as the MW liaison ...

Biogen

Director, Medical Writing - WCH

$191K - $263K/yr

About This Role: As the Director of Medical Writing for the West Coast Hub (WCH) you are ... Mentor and provide professional development guidance to junior writers. May serve as the MW liaison ...

Biogen

Director, Medical Writing - WCH

$191K - $263K/yr

About This Role: As the Director of Medical Writing for the West Coast Hub (WCH) you are ... Mentor and provide professional development guidance to junior writers. May serve as the MW liaison ...

Amgen

Regulatory Writing Sr Mgr

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 ...

Jj

Manager Medical Writing XTA

Raritan, NJ · On-site +1

Coaching or mentoring more junior staff on document planning, processes, content, and provide peer review as needed; overseeing the work of other medical writers, external contractors, and document ...

Jj

Manager Medical Writing XTA

Horsham, PA · On-site +1

Coaching or mentoring more junior staff on document planning, processes, content, and provide peer review as needed; overseeing the work of other medical writers, external contractors, and document ...

Travere

Associate Director, Medical Writing

San Diego, CA · On-site +1

Department: 517050 Medical Writing - TTIL Location: San Diego, United Kingdom - Remote, USA- Remote ... Mentor junior writers as applicable. * Develop, maintain, and drive document finalization timelines ...

Travere

Associate Director, Medical Writing

OR · On-site +1

Department: 517050 Medical Writing - TTIL Location: San Diego, United Kingdom - Remote, USA- Remote ... Mentor junior writers as applicable. * Develop, maintain, and drive document finalization timelines ...

Healthcare

Medical Writing III

$137K - $167K/yr

Reports to the Medical Information and Publications Manager and may provide training or supervision to junior writers or contractors as needed. * Participates or leads publication panel planning ...

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Junior Medical Writing information

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How much do junior medical writing jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for junior medical writing in the United States is $30.58, according to ZipRecruiter salary data. Most workers in this role earn between $22.84 and $30.77 per hour, depending on experience, location, and employer.

What is a junior medical writer?

A Junior Medical Writer is an entry-level professional who assists in creating scientific documents, such as clinical study reports, regulatory submissions, and medical publications. They work under the supervision of senior medical writers or project managers, ensuring the accuracy and clarity of medical information. Junior Medical Writers often collaborate with researchers, clinicians, and regulatory teams to gather data and present it in a clear, compliant manner. This role typically requires strong writing skills, a background in life sciences, and attention to detail.

What types of projects and documents are typically assigned to a junior medical writer, and how are these prioritized within a medical writing team?

As a Junior Medical Writer, you will often work on tasks such as drafting clinical study protocols, patient information sheets, regulatory submission documents, and literature summaries. These projects are usually assigned based on team deadlines, your prior experience, and the complexity of each document. Junior writers often begin with supporting sections or less complex tasks, receiving guidance from senior writers and project managers. Collaboration and regular feedback are key, helping you build expertise while ensuring high-quality deliverables that meet regulatory and scientific standards.

What are the key skills and qualifications needed to thrive as a junior medical writer, and why are they important?

To thrive as a Junior Medical Writer, you need a strong grasp of scientific and medical concepts, excellent written communication, and typically a life sciences degree. Familiarity with referencing software (like EndNote), Microsoft Office Suite, and guidelines such as ICH or AMA style is often required. Attention to detail, time management, and the ability to collaborate with multidisciplinary teams are valuable soft skills. These competencies ensure the production of accurate, compliant, and effective medical documents that support research, regulatory submissions, and healthcare communications.

What is the difference between Junior Medical Writing vs Medical Writing?

AspectJunior Medical WritingMedical Writing
Required CredentialsBachelor's degree, training in medical or life sciencesBachelor's or higher in life sciences, with experience or certification preferred
Work EnvironmentEntry-level, supporting senior writers, often in pharmaceutical or biotech companiesProfessional, independent or team-based, in healthcare, pharma, or CRO settings
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsSame as Junior Medical Writing, with broader scope and experience
Search & Comparison IntentUnderstanding entry-level roles in medical writingSeeking experienced medical writers or career progression

Junior Medical Writers typically have less experience and focus on supporting senior writers in creating clinical, regulatory, or marketing documents. Medical Writers are more experienced, often handling complex projects independently. The roles overlap in industry and credentials but differ mainly in experience level and scope of responsibilities.

More about Junior Medical Writing jobs

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Cities with the most Junior Medical Writing job openings:

What are the most commonly searched types of Medical Writing jobs?

The most popular types of Medical Writing jobs are:

What states have the most Junior Medical Writing jobs?

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What job categories do people searching Junior Medical Writing jobs look for?

The top searched job categories for Junior Medical Writing jobs are:

Junior Medical Writing jobs near you
Infographic showing various Junior Medical Writing job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $63,608 per year, or $30.6 per hour.

Senior Staff Medical Writer (Remote)

Stryker

Seattle, WA • On-site, Remote

$143K - $238K/yr

Full-time

Posted 3 days ago

New

Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

130th of 493 rated machine equipment manufacturers

Job description

Work Flexibility: Remote

Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based remotely anywhere within the United States. Stryker is one of the world's leading medical technology companies and, together with its customers, is driven to make healthcare better. Our Endoscopy Division delivers a diverse array of innovative medical technologies to support minimal invasive surgery through brilliant visualization, connected OR solutions, sports medicine products to sustainability solutions.

As the Senior Staff Medical Writer, you will develop scientific and clinical documentation that supports global regulatory compliance and market access for medical devices. This position partners closely with Regulatory Affairs, Clinical Affairs, Quality, Research & Development, and Marketing teams to translate complex clinical evidence into high-quality regulatory and scientific documents throughout the product lifecycle.

What You Will Do

  • Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF) documents, and other clinical evidence documentation supporting international product registrations and lifecycle management.

  • Compile, analyze, and synthesize clinical evidence from clinical studies, published literature, post-market data, and other safety and performance sources into submission-ready regulatory documents.

  • Respond to notified body reviews and regulatory feedback, driving resolution of clinical documentation questions to support ongoing market access.

  • Collaborate with cross-functional teams to develop clinical evidence strategies, regulatory documentation plans, and project timelines.

  • Author clinical study protocols, study reports, data summaries, and supporting scientific documents for regulatory and clinical initiatives.

  • Conduct systematic literature reviews, evaluate scientific data, and integrate findings into clinical and regulatory documentation.

  • Lead document review cycles, coordinate stakeholder feedback, resolve content issues, and obtain timely approvals.

  • Drive continuous improvement initiatives, maintain medical writing tools and templates, and mentor junior medical writing team members.

What You Need

Required

  • Bachelor's degree in a scientific, technical, healthcare, or related discipline.

  • Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals, or healthcare products.

  • Minimum 4 years of experience in scientific writing, medical writing, clinical research, or related regulatory documentation activities.

  • Experience authoring Clinical Evaluation Reports (CERs) and Post-Market Clinical Follow-Up (PMCF) documentation.

  • Expert knowledge of MEDDEV 2.7/1 Rev. 4, European Union Medical Device Regulation (EU MDR 2017/745), and Medical Device Coordination Group (MDCG) guidance for clinical evaluations.

  • Experience conducting systematic literature reviews and utilizing scientific databases, literature search methodologies, and literature management tools.

  • Knowledge of FDA, Good Clinical Practice (GCP), ISO 14155, ISO 14971, and applicable international medical device regulations and standards.

Preferred

  • Master's degree, PhD, PharmD, MD, MPH, RN, BSN, or other advanced health-related degree.

  • Experience authoring clinical study protocols, clinical study reports, manuscripts, or scientific publications.

  • Experience supporting regulatory submissions and global market access initiatives for medical devices.

  • Knowledge of clinical operations, risk management, and international regulatory requirements.

United States of America Pay Ranges:

  • USN: $110,100 - $183,400 USD Annual
  • US5: $115,600 - $192,600 USD Annual
  • US10: $121,100 - $201,700 USD Annual
  • US15: $126,600 - $210,900 USD Annual
  • US20: $132,100 - $220,100 USD Annual
  • US30: $143,100 - $238,400 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.

Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.

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