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Senior Medical Writer Jobs in Raleigh, NC (NOW HIRING)

Air Clean Systems

Senior Chemist

Creedmoor, NC · On-site

CS Medical Job Title : Senior Chemist Department or Division : Science Reports To : Director of ... Create and write validations, test protocols, procedures, reports, and proposals * Review and ...

Next Step Systems

Senior Firmware Engineer

Durham, NC · On-site

$115K - $152K/yr

... verbal and written communications skills; strong computer skills. - Experience implementing DSP ... Benefits include medical insurance, retirement plan, PTO, etc. Salary: 80K+ DOE. Keywords: Durham ...

Red Hat, LLC

Senior Software Engineer

Raleigh, NC · On-site

$150 - $200/hr

Good written and verbal communication in English. Preferred Skills * Experience with an autonomous ... Comprehensive medical, dental, and vision coverage * Flexible Spending Account - healthcare and ...

Cutera-Inc

Senior Industrial Designer

Raleigh, NC · On-site

$100 - $125/hr

This position will play a key role in shaping the next generation of medical and aesthetic ... Excellent verbal, written, and visual communication skills.Ability to synthesize technical, user ...

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Senior Medical Writer information

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$34K

$133.5K

$240.6K

How much do senior medical writer jobs pay per year?

As of Sep 7, 2026, the average yearly pay for senior medical writer in Raleigh, NC is $133,454.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,100.00 and $161,400.00 per year, depending on experience, location, and employer.

What is a senior medical writer?

A Senior Medical Writer is responsible for creating clear, accurate, and compliant medical documents, including regulatory submissions, clinical study reports, and scientific publications. They work closely with cross-functional teams, such as medical affairs, regulatory affairs, and clinical teams, to ensure high-quality content. Senior Medical Writers also review and edit documents for consistency, clarity, and adherence to industry guidelines. Often, they mentor junior writers and contribute to process improvements within the medical writing team.

What are the key skills and qualifications needed to thrive as a senior medical writer?

To thrive as a Senior Medical Writer, you need advanced writing and editing skills, a thorough understanding of scientific and medical concepts, and typically a degree in a life science or related field. Familiarity with referencing tools (like EndNote), document management systems, and compliance with regulatory guidelines (such as ICH or FDA standards) is often required. Strong attention to detail, project management abilities, and the capacity to communicate complex ideas clearly are important soft skills for this position. These competencies ensure accurate, high-quality medical content that meets industry standards and supports effective communication among healthcare professionals and stakeholders.

What are some common challenges faced by senior medical writers, and how can they be addressed?

Senior Medical Writers often encounter challenges such as managing tight deadlines, interpreting complex scientific data, and ensuring adherence to strict regulatory requirements. To navigate these challenges, it's essential to have strong organizational skills, effective communication with project teams, and a solid grasp of industry guidelines. Many Senior Medical Writers find that staying current with new regulations, participating in ongoing professional development, and leveraging collaborative tools help streamline the workflow. By proactively addressing these challenges, writers can maintain accuracy and efficiency while contributing valuable expertise to cross-functional teams.

What are the most commonly searched types of Medical Writer jobs in Raleigh, NC?

The most popular types of Medical Writer jobs in Raleigh, NC are:

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For Senior Medical Writer jobs in Raleigh, NC, the most frequently searched job titles are:

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Senior Medical Writer jobs near you
Infographic showing various Senior Medical Writer job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $133,454 per year, or $64.2 per hour.

Senior Chemist

Air Clean Systems

Creedmoor, NC • On-site

Full-time

Re-posted 11 days ago

Key responsibilities

  • Develop and oversee the chemistry aspects of projects and assays to support medical device and product development.

  • Research, develop, and improve scientific methods, assays, and analytical processes, including the operation of HPLC equipment.

  • Create and write validations, test protocols, procedures, reports, and proposals related to scientific activities.

Job description

Job Description

 

CS Medical

 

 

Job Title: Senior Chemist 

 

Department or Division:  Science  

 

Reports To:  Director of Laboratory Operations

 

 

JOB TASKS, DUTIES, AND RESPONSIBILITIES

As a member of the Science team at CS Medical, the Senior Chemist position is responsible for developing and overseeing the chemistry aspects of projects and assays to support the development of current and future medical devices and products. Reporting to the Director of Laboratory Operations, the Senior Chemist works with laboratory staff and adheres to schedules to ensure project completion. Your first and foremost goal will always be the safety of yourself and other CS Medical personnel in the performance of your duties.

JOB DUTIES: 
 

  • Research and development to help support and develop products and devices
  • Lead product development projects 
  • Develop new scientific methods and assays
  • Improve and customize current products, formulations and analytical methods and processes
  • Create and write validations, test protocols, procedures, reports, and proposals
  • Review and evaluate analysis data concerning the needs, requirements, and operation for (test) project design and support
  • Review and evaluate scientific methods, procedures, data, and articles/journals
  • Determine the relationships of chemical and physical properties, composition, structures and reactions of compounds using chromatography, spectrophotometry and spectroscopy techniques
  • Performs applied scientific analysis and activities relative to the research, design and development of lab and field projects
  • Operation of Liquid Chromatography instrumentation (HPLC)
  • Stay current and comply with various regulatory agencies
  • Maintain equipment, supplies, and chemicals
  • Ensure health and safety within the laboratory

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

 

 

MINIMUM QUALIFICATIONS

  • B.S. or B.A. in Chemistry, Biochemistry or related discipline
  • Minimum of five years of experience in a chemistry or related laboratory
  • Minimum of five years with HPLC work and development of assays
  • Minimum of five years of product development
  • Ability to lead projects
  • Experience working in a laboratory setting, analytical skills, sample extraction and analysis, titrations, experience with bioanalytical methods, HPLC, spectrophotometry
  • Ability to interpret analysis from outside sources (example: HPLC, GC, validations, etc.)
  • PC skills and ability to learn new software, systems, and programs
  • Ability to effectively communicate and interact with technical staff at all levels in a team-based environment
  • Detail and quality oriented
  • Ability to work independently
  • Willingness to travel in the US occasionally
  • Working knowledge of Quality Assurance and Good Laboratory Practices 

PREFERRED QUALIFICATIONS

  • Masters in chemistry or biochemistry
  • Experience with FDA, EU, EPA, and Health Canada submissions
  • Medical device experience
  • HPLC and GC experience
  • Liquid chemical sterilant and/or high-level disinfectant experience
     
     

Accountabilities
 

  • Project deadlines are timely met
  • Research and development of new methods and assays
  • Research and development for current or new products
  • Recording, analyzing and interpreting data
  • Write validations, methods, protocols and reports
  • Keeping up to date with scientific and research developments
  • Maintaining a safe work environment

 

LOCATION

This position will be based at our Creedmoor, NC office.