Medical Writer Jobs
Medical Writer jobs are open across pharmaceutical, biotech, medical device, and clinical research industries, from entry-level associate to principal and director, with specializations in regulatory writing, clinical documentation, and medical communications. Find a role that fits from the openings below and apply directly.
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INTRODUCTION
Located in Redmond WA, SystImmune, Inc. is a biopharmaceutical company focused on treating cancer through developing novel therapeutic multi-specific antibodies and antibody-drug conjugates (ADCs). Our objective is to create biologics that work through systematic intervention on the solid tumor micro-environment, to either directly attack the tumor or to activate the immune system to attack the tumor.
Position Summary:
The medical writer will be responsible for the management and oversight of assigned medical writing projects, including clinical study protocols and reports, investigational new drug applications (INDs), investigator brochures, reviewing informed consent forms and regulatory briefing materials. They will be accountable for ensuring that all documents are written according to established templates and guidance, and that they are of the highest quality with respect to scientific content, organization, accuracy, regulatory guidelines, clarity of presentation, and structure.
Key Responsibilities:
- Write, edit and/or manage the production of high-quality clinical documentation including clinical study protocols, synopses, and clinical study reports for submission to regulatory authorities in support of marketing applications and BLAs.
- Act as a member of clinical trial teams
- Follow and track clinical documentation milestones
- Write/edit other strategic documents, as required
Required Qualifications:
- Master's degree in a life sciences discipline or at least 3 to 4 years of experience as a medical writer in the pharmaceutical industry; PhD with at least 1 year experience as a medical writer in the pharmaceutical industry
- Excellent writing and effective communication skills
- Proven interpersonal, organizational and problem-solving skills in a matrix management environment
- Knowledge of FDA and ICH guidelines
- Skilled in clinical data interpretation
- Proven experience writing/supporting major documents (e.g., protocols, CSRs, ISE, ISS, and Clinical Overview etc.)
Preferred Qualifications:
- Knowledge of drug development and regulatory requirements to guide document organization
- Project management experience including the use of negotiation and influence to ensure document timelines are met while maintaining high quality
The hiring pay range for this position is $80,000 - $130,000 per year based on skills, education, and experience relevant to the role.
SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs).
SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discovery or IND-enabling stages, representing cutting-edge biologics development.
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
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Find Medical Writer JobsMedical Writer Job Market
A snapshot from current openings nationwide, updated as new roles post.
Who's Hiring
- Syneos Health8

- BioMarin Pharmaceutical7

- Laborie7

- Precision Medicine5

- Ionis Pharmaceuticals3

Top Industries Hiring
- Biotechnology & Pharmaceuticals27
- Healthcare & Medical Services12
- Science & Research12
- Consulting & Professional Services7
- Distribution & Wholesale7
What Employers Look For
The qualifications that appear most often in medical writer jobs.
- Bachelor's or advanced degree in life sciences, pharmacy, or a related scientific field
- Demonstrated experience writing clinical study reports, regulatory submissions, or medical communications
- Proficiency with Microsoft Word styles, templates, and tracked-changes workflows
- Familiarity with ICH guidelines, FDA or EMA submission requirements, and Good Documentation Practice
- Strong ability to interpret and translate clinical data for scientific and non-scientific audiences
- American Medical Writers Association certification (AMWA) or equivalent credential preferred
Tips for Your Medical Writer Job Search
Tailor your resume to document type
Hiring managers scan for the specific document types you've written: CSRs, IBs, SmPCs, manuscripts, or MOA decks. Lead with a short document portfolio list under your summary so recruiters immediately see whether your experience matches the role's output.
Apply early to roles that fit
Migrate Mate lists medical writer openings from across the United States in one place, so you can find roles that match and apply directly to each listing.
Highlight therapeutic area depth strategically
Most postings specify a TA like oncology, rare disease, or cardiovascular. If your background crosses multiple areas, foreground the one that matches each role rather than listing all of them equally, diffuse coverage reads as a lack of specialization.
Prepare a writing sample before interviewing
Many medical writer interviews include a writing exercise or a request for a sample before the second round. Have a clean, de-identified CSR summary or manuscript excerpt ready so you're not scrambling after a callback.
Address regulatory experience in your cover letter
Regulatory-track roles at CROs and pharma companies weight ICH, FDA, or EMA guideline familiarity heavily. If you've worked under those frameworks, name the specific guidelines you've applied rather than describing it as general regulatory experience.
Negotiate scope not just salary
When you reach the offer stage, ask specifically about document ownership, review cycle expectations, and whether medical information or publication planning work is included. Scope creep is common in this role and understanding it upfront protects you after you start.
Medical Writer Jobs: Frequently Asked Questions
Which companies are hiring the most medical writers?
The companies hiring the most medical writers right now include Syneos Health, BioMarin Pharmaceutical, and Laborie, with the largest share of openings in California, Massachusetts, and New Jersey, based on current listings on Migrate Mate as of June 2026. Demand is consistently strongest at large CROs, integrated pharma companies, and medical communications agencies.
How many medical writer jobs are remote?
About 32% of medical writer openings are fully remote or hybrid as of June 2026, making it one of the more location-flexible roles in the life sciences. Regulatory writing and publication planning positions tend to skew most remote, while roles tied to on-site clinical teams or manufacturing sites are more likely to require in-person attendance.
How do you become a medical writer?
Start by earning a degree in a life science, pharmacy, nursing, or health communications field, then build writing samples by contributing to research publications, patient-facing materials, or science communication projects. Pursue AMWA membership for resources and credentialing, then target entry-level associate roles at CROs or medical communications agencies where mentorship and document variety are highest.
Can you get a medical writer job with little experience?
Yes, entry-level medical writer roles do exist, particularly at CROs and medcomms agencies that train associates internally. The strongest candidates without direct industry experience come in with published research, thesis writing, or healthcare content backgrounds, and bring a polished writing sample that shows they can translate scientific data into clear, structured prose.
What does the medical writer interview process look like?
Most medical writer interviews run two to three rounds. The first is typically a recruiter screen focused on therapeutic area background and document experience. The second is a hiring manager interview covering writing process and regulatory familiarity. Many companies add a written exercise asking you to summarize a study abstract or edit a draft document before a final offer conversation.
Where can I find and apply to medical writer jobs?
You can find and apply to medical writer jobs on Migrate Mate, which lists current openings from across the United States in one place. Search the listings to find roles that match your therapeutic area experience and document background, then apply directly to each one that fits.
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