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Evening Senior Medical Writer Jobs (NOW HIRING)

Work Schedule Standard (Mon-Fri) Environmental Conditions Office ​Join Us as a Senior Medical Writer - Make an Impact at the Forefront of Innovation Provides high-quality medical and scientific ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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

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

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

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 ...

Showing results 21-40

Evening Senior Medical Writer information

See salary details

$35K

$137.3K

$247.5K

How much do evening senior medical writer jobs pay per year?

As of Aug 11, 2026, the average yearly pay for evening 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.
What cities are hiring for Evening Senior Medical Writer jobs? Cities with the most Evening 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:
What states have the most Evening Senior Medical Writer jobs? States with the most job openings for Evening Senior Medical Writer jobs include:
Infographic showing various Evening 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.

Full-time

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Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 423 frontline employees who took The Breakroom Quiz

197th of 538 rated manufacturers


Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

​Join Us as a Senior Medical Writer - Make an Impact at the Forefront of Innovation

Provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. Demonstrates subject matter and therapeutic area expertise. May function as a project lead. Collaborates with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.
What You'll Do:
• Serve as primary author who writes and provides input on routine documents such as Medical Information Response Documents and Questions and Answers.

• May research, write or edit complex clinical and scientific and program level documents, including AMCP dossiers and Infographics.
• Review routine documents prepared by junior team members. May provide training and mentorship for junior writers on document preparation, the use of software for document development, document types, and therapeutic area knowledge.
• Ensure compliance with quality processes and requirements for assigned documents. Provide input on and independently develops best practices, methods and techniques for achieving optimal results, including various client specific processes.

• May function as a project lead or assist with program management activities. Duties could include developing timelines, budgets, forecasts, and contract modifications; tracking deliverable metrics; and representing medical writing team in client meetings.    


Education & Experience Requirements:
• Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Advanced degree preferred
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
• Experience working in the pharmaceutical/CRO industry preferred
• Additional qualifications in medical writing or medical information advantageous
Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.
Knowledge, Skills, Abilities:
• Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills
• Strong project management skills
• Excellent interpersonal skills including problem solving
• Strong negotiation skills
• Excellent oral and written communication skills with strong presentation skills
• Significant knowledge of global, regional, national and other document development guidelines
• In-depth knowledge in a specialty area such as preclinical, therapeutic, regulatory submissions, communications, etc.
• Great judgment and decision-making skills
• Excellent computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook)
Working Conditions and Environment:
• Work is performed in an office environment.
• Exposure to electrical office equipment.
• Occasional drives to site locations with occasional travel both domestic and international.
• Long, varied hours required occasionally.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthroughs.


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