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Full Time Senior Medical Writer Jobs (NOW HIRING)

Argenx

Senior Medical Writer

$104K - $143K/yr

For the expansion of our team, argenx is looking for a Senior Medical Writer who will provide medical writing support for developing complex clinical, nonclinical, and safety documents for regulatory ...

Medtronic

Senior Medical Writer

North Haven, CT · On-site +1

We are seeking a Senior Medical Writer to join the Clinical Evaluation team in support of the Core Surgical Innovation business. In this role, the Senior Medical Writer will be responsible for ...

Regeneron Pharmaceuticals, Inc.

Senior Medical Writer

$128K - $210K/yr

We are seeking a Senior Medical Writer to join our Medical Writing team, supporting clinical document delivery across Global Development in a remote work mode. In this role, you will author clinical ...

Medtronic

Senior Medical Writer

North Haven, CT · On-site +1

We are seeking a Senior Medical Writer to join the Clinical Evaluation team in support of the Core Surgical Innovation business. In this role, the Senior Medical Writer will be responsible for ...

Synchrony Group

Senior Medical Writer

West Chester, PA · On-site

The Senior Medical Writer: 1) writes original content for publications activities, and other materials for healthcare professional (HCP) and internal client audiences; 2) demonstrates a command of ...

Synchrony Group

Senior Medical Writer

West Chester, PA · On-site +1

The Senior Medical Writer: 1) writes original content for publications activities, and other materials for healthcare professional (HCP) and internal client audiences; 2) demonstrates a command of ...

Synchrony Group

Senior Medical Writer

West Chester, PA · On-site

The Senior Medical Writer: 1) writes original content for publications activities, and other materials for healthcare professional (HCP) and internal client audiences; 2) demonstrates a command of ...

Syneos Health

Sr. Medical Writer (Regulatory)

Sr. Medical Writer (Regulatory) Syneos Health ® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point ...

ProPharma Group

Senior Medical Writer

Charleston, WV · On-site

With minimal supervision, authors (writes/edits) high-quality medical writing deliverables (i.e., clinical, safety, regulatory, device, diagnostics, or disclosures documents) across all phases of ...

CEDENT

Senior Medical Writer

Rockville, MD · On-site

The Medical Writer collaborates with members of cross-functional teams to prepare high-quality protocols, investigator brochures, synopses, regulatory documents, clinical publications, and related ...

Artivion

Senior Medical Writer

Kennesaw, GA

Communicate with physicians, vendors, and other medical experts. * Report on adverse events, complaints, and failures associated with the product line identified through the writing process

CryoLife

Senior Medical Writer

Kennesaw, GA · On-site

Communicate with physicians, vendors, and other medical experts. * Report on adverse events, complaints, and failures associated with the product line identified through the writing process

OSI Pharmaceuticals

Senior Medical Writer

Boulder, CO · On-site

Degree should be in biological science, English or other relevant area. 5 to 7 years directly related medical writing experience. Outstanding writing, analytical and research skills a must. Ability ...

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Full Time Senior Medical Writer information

See salary details

$35K

$137.3K

$247.5K

How much do full time senior medical writer jobs pay per year?

As of Aug 10, 2026, the average yearly pay for full time senior medical writer in the United States is $137,286.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,000.00 and $166,000.00 per year, depending on experience, location, and employer.

Is there a demand for full time senior medical writers?

There is a strong and growing demand for full-time senior medical writers due to the increasing need for clear scientific communication in the healthcare and pharmaceutical industries. These roles often require expertise in medical terminology, regulatory guidelines, and proficiency with tools like reference management software. The demand is driven by ongoing clinical research, drug development, and regulatory submission processes.

Do full time senior medical writers make good money?

Full-time senior medical writers typically earn a competitive salary that reflects their experience, expertise, and the complexity of medical writing tasks. Salaries often range from $80,000 to over $150,000 annually, depending on the industry, location, and whether they work in pharmaceutical, biotech, or healthcare communications. They may also receive benefits such as bonuses, health insurance, and professional development opportunities.

How much do full time senior medical writers make in the US?

Full-time senior medical writers in the US typically earn between $100,000 and $150,000 annually, depending on experience, location, and employer. They often possess advanced degrees in life sciences and strong writing skills, with some roles offering additional benefits or bonuses.
More about Full Time Senior Medical Writer jobs
What cities are hiring for Full Time Senior Medical Writer jobs? Cities with the most Full Time Senior Medical Writer job openings:
What are the most commonly searched types of Senior Medical Writer jobs? The most popular types of Senior Medical Writer jobs are:
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Full Time Senior Medical Writer jobs near you
Infographic showing various Full Time Senior Medical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $137,286 per year, or $66 per hour.

Senior Medical Writer

Argenx

Remote

$104K - $143K/yr

Full-time

Medical, Retirement

Re-posted 5 days ago

Job description

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases.
We are building a new kind of biotech company, one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our business. We strive to inspire and grow our company, our partnerships, our science, and our people, because when we do, we deliver more for patients.
For the expansion of our team, argenx is looking for a Senior Medical Writer who will provide medical writing support for developing complex clinical, nonclinical, and safety documents for regulatory submissions.
This individual will execute the overall strategy for all medical writing processes according to argenx medical writing standards and corporate objectives.
Key Accountabilities/Responsibilities:
  • Author and project manage SME contribution to develop content for regulatory submissions that is well-organized, consistent, accurate, and compliant with argenx Medical Writing standards, including style guide, lexicon, templates, and libraries
  • Authors content for phase 1-4 protocols, master ICFs, IBs, and CSRs
  • Responsible for inspection-readiness of medical writing activities
  • Supports the lead writer and project teams to ensure project deadlines are met
  • Executes corporate objectives, goals, measures, and strategies
  • Capable of working on multiple deliverables simultaneously

Desired Skills and Experience:
  • Bachelor's degree in a scientific or clinical discipline or related field is required; Ph.D. preferred
  • Minimum of 3 years of related, sponsor-level pharma or biotech clinical/regulatory medical writing experience required; CRO experience considered
  • Native/bilingual or fluent American English proficiency
  • Solution-focused
  • Experience with Veeva Vault and Please Review
  • Experience with implementing lean writing techniques
  • Basic understanding of scientific methodology as applied to drug development, including the phases, processes, and techniques used within a clinical development environment from protocol design through regulatory submission
  • Familiarity with pharmacovigilance guidelines and developing aggregate reports
  • Ability to work precisely according to procedures and regulations
  • Ability to prioritize and multi-task successfully in a fast-paced environment
  • Ability to work autonomously, as well as in a team
  • Excellent written and verbal communication skills
  • Excellent time management skills and a proven ability to work on multiple projects at any given time
  • Must be proficient in MS Office

For applicants in the United States: The annual base salary hiring range for this position is $104,000.00 - $143,000.00 USD. This range reflects our good faith estimate at the time of posting. Individual compensation is determined using objective, inclusive, and job-related criteria such as relevant experience, skills, demonstrated competencies and internal equity. This means actual pay may differ from the posted range when justified by these factors. Because market conditions evolve, pay ranges are reviewed regularly and may be adjusted to remain aligned with external benchmarks.
This job is eligible to participate in our short-term and long-term incentive programs, subject to the terms and conditions of those plans and applicable policies. It also includes a comprehensive benefits package, including but not limited to retirement savings plans, health benefits and other benefits subject to the terms of the applicable plans and program guidelines.
At argenx, all applicants are welcomed in an inclusive environment. They will receive equal consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other applicable legally protected characteristics. argenx is proud to be an equal opportunity employer.
Before you submit your application, CV or any other personal details to us, please review our argenx Privacy Notice for Job Applicants to learn more about how argenx B.V. and its affiliates ("argenx") will handle and protect your personal data. If you have any questions or you wish to exercise your privacy rights, please contact our Global Privacy Office by email at privacy@argenx.com.
If you require reasonable accommodation in completing your application, interviewing, or otherwise participating in the candidate selection process please contact us at hr.us@argenx.com. Only inquiries related to an accommodation request will receive a response.

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