ZipRecruiter

Log In

1

Medical Writer Jobs in Michigan (NOW HIRING)

MMS

Senior Medical Writer (Remote)

Canton, MI · On-site

Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical ...

Gopuff

MI - Detroit

Detroit, MI · On-site

With Gopuff, you don't have to worry about which restaurant to go to or where your next ride will take you. It's quick and easy to earn on your time, delivering the essentials people need. Want to ...

Learning Care Group

Proposal Writer

Novi, MI · On-site

Position Summary The Proposal Writer is responsible for developing high-quality, compelling ... medical, dental, vision, healthcare & dependent care flexible spending accounts (FSAs), life ...

Corewell Health

Grant Writer

Southfield, MI · On-site

Job Summary The Grant Writer, Corporate/Foundation Giving and Public Support is responsible for ... Coordinate grant processing, maintaining contact with Community Health and appropriate medical ...

Kforce Technology Staffing

Tech Writer

Clawson, MI · On-site

The main function of a Technical Writer is to write technical materials, such as equipment ... We offer comprehensive benefits including medical/dental/vision insurance, HSA, FSA, 401(k), and ...

Spectrum Health

Grant Writer

Southfield, MI · Hybrid

Job Summary The Grant Writer, Corporate/Foundation Giving and Public Support is responsible for ... Coordinate grant processing, maintaining contact with Community Health and appropriate medical ...

KBR, Inc.

Technical Writer

Sterling Heights, MI · On-site

Technical Writer Program Summary KBR's Defense & Technology Solutions (DTS) business unit combines ... with company match, medical, dental, vision, life insurance, AD&D, flexible spending account ...

KBR

Technical Writer

Sterling Heights, MI

Technical Writer Program Summary KBR's Defense & Technology Solutions (DTS) business unit combines ... with company match, medical, dental, vision, life insurance, AD&D, flexible spending account ...

FastTek

Technical Writer

Warren, MI

Technical Writer #1058332 The energy at our company is contagious. We're driven by our immense ... Medical and Dental (FastTek pays majority of the medical program) * Vision * Personal Time Off (PTO ...

Codetech Inc

Technical Writer

Lansing, MI · On-site

Technical Writer 3, DTMB Agency Services Supporting MDARD DTMB Agency Services is seeking a Technical Writer 3 to support agency initiatives to review and update documents and web published content ...

FastTek

Technical Writer

Clawson, MI

Technical Writer #1060902 The energy at our company is contagious. We're driven by our immense ... Medical and Dental (FastTek pays majority of the medical program) * Vision * Personal Time Off (PTO ...

1 point system

Technical Writer

Lansing, MI · On-site

• 5+ years of experience in technical writing and editing for the software development industry. • 4+ years of experience in technical writing and editing for the financial industry. • 4+ years ...

next page

Showing results 1-20

All JobsMedical Writer JobsMedical Writer Jobs in Michigan

Medical Writer information

See Michigan salary details

$10

$40

$68

How much do medical writer jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for medical writer in Michigan is $40.33, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $48.80 per hour, depending on experience, location, and employer.

Do you need a PhD to be a Medical Writer?

A PhD is not required to become a Medical Writer, but many professionals in the field hold advanced degrees such as a master's or doctorate. Strong writing skills, a background in life sciences or healthcare, and familiarity with scientific literature are essential for success in this role.

What are medical writers?

Medical writers are professionals who create scientific documents related to healthcare, medicine, and the life sciences. They produce materials such as clinical study reports, journal articles, regulatory submissions, and educational content for healthcare professionals or the public. Medical writers must have a strong understanding of medical terminology, research methods, and regulatory guidelines. Their work helps communicate complex scientific information clearly, accurately, and in compliance with industry standards.

Do medical writers make good money?

Medical writers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start around $60,000 annually, while experienced professionals can earn over $100,000, especially with specialized knowledge or certifications. The role often involves working with scientific data, regulatory documents, and medical publications.

What Is the Job of a Medical Writer?

Medical writers create scientific documents and articles. This can include a variety of different types of papers, including research documents, educational or promotional literature, articles, and abstracts. You may ghostwrite for well-known physicians and scientists, or you may write under your own name, depending on what field you are in. Other medical writer jobs include journalists for medical magazines, authors of books, and those who write marketing materials for health care organizations. Regardless of your specialty, you must be able to interpret complex scientific information and create articles that people can read and understand, particularly when writing for the general public.

What is a Medical Writer?

A medical writer is a professional who creates scientific and medical documents such as research articles, regulatory submissions, and clinical trial reports. They combine expertise in medicine or life sciences with strong writing skills to communicate complex information clearly and accurately, often working in pharmaceutical, biotech, or healthcare industries.

What are the key skills and qualifications needed to thrive as a Medical Writer, and why are they important?

To thrive as a Medical Writer, you need a strong background in life sciences or medicine, excellent written communication skills, and often an advanced degree such as a PhD, MD, or relevant certification. Familiarity with reference management software, medical literature databases, and regulatory guidelines like ICH or GPP is typically required. Attention to detail, the ability to interpret complex data, and collaboration skills set standout professionals apart in this role. These competencies ensure the production of accurate, compliant, and accessible medical documents crucial for regulatory approval, education, and communication in healthcare.

What is the difference between Medical Writer vs Clinical Writer?

AspectMedical WriterClinical Writer
CredentialsTypically requires a degree in life sciences, healthcare, or related fields; certifications like AMWA or EMWA are commonSimilar credentials; often holds degrees in life sciences with certifications in clinical research or writing
Work EnvironmentWorks in pharmaceutical, biotech, or healthcare companies, often in offices or remote settingsPrimarily in clinical research organizations, pharmaceutical companies, or hospitals, often in office or remote settings
Industry UsageUsed across pharma, biotech, medical device industries for regulatory, educational, and promotional contentFocused on clinical trial documentation, protocols, and reports within clinical research

Medical Writers and Clinical Writers share similar backgrounds and work environments, often collaborating in healthcare and pharmaceutical sectors. The main difference lies in their focus: Medical Writers create a broad range of medical content, while Clinical Writers specialize in clinical trial documentation and reports.

How do I become a Medical Writer?

To become a medical writer, typically a bachelor's degree in life sciences, healthcare, or a related field is required, often supplemented by advanced degrees or certifications in medical writing or regulatory writing. Gaining experience through internships, developing strong writing skills, and becoming familiar with industry guidelines and tools like reference management software can improve job prospects.

How does a Medical Writer typically collaborate with subject matter experts during a project?

Medical Writers frequently work closely with physicians, researchers, and regulatory specialists to ensure content accuracy and clarity. This collaboration often involves conducting interviews, reviewing scientific data, and incorporating expert feedback into drafts. Building strong professional relationships and maintaining clear communication are key for efficiently resolving technical questions and aligning final documents with project objectives. This teamwork is essential for producing high-quality, compliant materials that meet both scientific and regulatory standards.
More about Medical Writer jobs
What are the most commonly searched types of Medical Writer jobs in Michigan? The most popular types of Medical Writer jobs in Michigan are:
What are popular job titles related to Medical Writer jobs in Michigan? For Medical Writer jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Medical Writer jobs in Michigan look for? The top searched job categories for Medical Writer jobs in Michigan are:
What cities in Michigan are hiring for Medical Writer jobs? Cities in Michigan with the most Medical Writer job openings:
What are popular job titles related to Medical Writer jobs in MI? For Medical Writer jobs in MI, the most frequently searched job titles are:
Medical Writer jobs near you
Infographic showing various Medical Writer job openings in Michigan as of July 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution, with an average salary of $83,878 per year, or $40.3 per hour.
Senior Medical Writer (Remote)

Senior Medical Writer (Remote)

MMS

Canton, MI • On-site

Full-time

Posted 2 days ago

Job description

About MMS
MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating.
Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.
Responsibilities
  • Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias
  • Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals
  • Complete writing assignments in a timely manner
  • Maintain timelines and workflow of writing assignments
  • Practice good internal and external customer service
  • Highly proficient with styles of writing for various regulatory documents
  • Expert proficiency with client templates & style guides
  • Interact directly and independently with client to coordinate all facets of projects; competent communicator skills for projects
  • Contribute substantially to, or manages, production of interpretive guides
  • Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary
  • Mentor medical writers and other members of the project team who are involved in the writing process
Requirements
  • At least 3 years of previous experience in the pharmaceutical industry
  • Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience
  • The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline
  • Substantial clinical study protocol experience, as lead author, required
  • Experience leading and managing teams while authoring regulatory documents with aggressive timelines
  • Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus
  • Understanding of clinical data
  • Exceptional writing skills are a must
  • Excellent organizational skills and the ability to multi-task are essential prerequisites
  • Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools
  • Experience being a project lead, or managing a project team
  • Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus
  • Not required, but experience with orphan drug designations and PSP/PIPs a plus

Powered by JazzHR

iGBtWzmcxC

M. M. S. logo

About M. M. S.

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

Los Angeles, CA, US

Year founded

1980

View All M. M. S. Jobs