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Clinical Writer Jobs in Michigan (NOW HIRING)

MMS

Senior Nonclinical Writer (US)

Canton, MI · On-site

This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. Roles and Responsibilities: * Strong ...

MMS Holdings Inc.

Nonclinical Writer

Canton, MI · On-site

Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, Investigator's Brochure [IB], Nonclinical Study Reports, Meeting Requests ...

Pharmacy Careers

Remote Clinical Review Pharmacist

Detroit, MI · On-site

$108K - $129K/yr

Excellent clinical writing, critical thinking, and communication. Why This Role? * 100% remote with flexible scheduling. * Help patients access safe, effective, and affordable medications. * Develop ...

MMS

Senior Medical Writer (Remote)

Canton, MI · On-site

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 ...

Bronson Healthcare

Senior Grant Writer

Kalamazoo, MI · On-site

This role serves as the Foundation's primary grant writing expert, managing a portfolio of ... Translate complex clinical programs, capital priorities, and community health initiatives into ...

micro1 AI

Medical Writing Manager

Grand Rapids, MI · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

micro1 AI

Medical Writing Manager

Detroit, MI · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

micro1 AI

Medical Writing Manager

Ann Arbor, MI · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

micro1 AI

Medical Writing Manager

Dearborn, MI · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

micro1 AI

Medical Writing Manager

Lansing, MI · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

micro1 AI

Medical Writing Manager

Warren, MI · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

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Clinical Writer information

See Michigan salary details

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How much do clinical writer jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for clinical writer in Michigan is $47.37, according to ZipRecruiter salary data. Most workers in this role earn between $34.76 and $55.96 per hour, depending on experience, location, and employer.

What is a clinical writer?

A Clinical Writer is a professional who creates, edits, and manages medical and scientific documents related to clinical research, healthcare, and pharmaceuticals. They often prepare clinical study reports, regulatory submissions, patient information leaflets, and scientific manuscripts. Clinical Writers work closely with researchers, physicians, and regulatory professionals to ensure that complex clinical information is communicated clearly, accurately, and in compliance with industry standards. Their work is essential for documenting clinical trials and supporting the approval of new drugs or therapies.

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

To thrive as a Clinical Writer, you need a solid background in life sciences or medical fields, excellent writing skills, and attention to detail, often supported by a relevant degree. Familiarity with regulatory guidelines, literature databases, and tools like EndNote, as well as certifications such as AMWA or EMWA, are highly valued. Strong communication, critical thinking, and time management help Clinical Writers convey complex information clearly and collaborate with medical professionals. These skills ensure the accuracy, clarity, and compliance of clinical documents critical for regulatory submissions and advancing medical knowledge.

What are some common challenges clinical writers face when translating complex medical research into accessible documents?

Clinical writers often encounter the challenge of interpreting highly technical and data-rich research while ensuring accuracy and regulatory compliance. Balancing the need for scientific precision with the ability to communicate information clearly to various audiences—such as healthcare professionals, regulatory agencies, or patients—requires strong analytical and communication skills. Additionally, clinical writers must stay updated on evolving guidelines and collaborate closely with subject matter experts, which can be demanding but also enriches their expertise and professional network.

Do clinical writers make good money?

Clinical 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 skills or certifications in regulatory writing or medical communications.

How can I get into clinical writing with no experience?

Clinical writers typically need strong writing skills, a background in life sciences or healthcare, and familiarity with regulatory guidelines. Gaining experience through internships, entry-level medical writing roles, or certification programs like the American Medical Writers Association can help build relevant skills and credibility for entry into the field.

Is there a demand for clinical writers?

There is a steady demand for clinical writers in the healthcare and pharmaceutical industries due to the need for clear documentation of clinical trial data, regulatory submissions, and medical communications. Opportunities are available in biotech, pharmaceutical companies, and contract research organizations, often requiring knowledge of regulatory guidelines and scientific writing skills.

What are popular job titles related to Clinical Writer jobs in Michigan?

For Clinical Writer jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Clinical Writer jobs in Michigan look for?

The top searched job categories for Clinical Writer jobs in Michigan are:

What are popular job titles related to Clinical Writer jobs in MI?

For Clinical Writer jobs in MI, the most frequently searched job titles are:

Clinical Writer jobs near you
Infographic showing various Clinical Writer job openings in Michigan as of August 2026, with employment types broken down into 3% As Needed, 68% Full Time, 18% Part Time, 2% Temporary, 8% Contract, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $98,532 per year, or $47.4 per hour.

Senior Nonclinical Writer (US)

Canton, MI • On-site

MMS
Pharmaceutical and Medicine Manufacturing • 1 - 10 employees
Learn more about MMSexternal

Full-time

Re-posted 26 days ago

Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
 
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. 

Roles and Responsibilities:

  • Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, 1st Edition Investigator’s Brochure [IB], Nonclinical Study Reports, Meeting Requests, Briefing Documents, RTQs).
  • Lead projects independently with minimal oversight, lead the writing (structure, content and messaging) of nonclinical submission documents for INDs/CTAs/NDAs/BLAs/MAAs, ensure the nonclinical package aligns with current regulatory guidelines and meets scientific integrity.
  • Ability to author based on highly technical sources such as GLP and non-GLP nonclinical study reports, in vivo and in vitro nonclinical data.
  • Ability to develop a mapping plan for the placement of nonclinical studies within structure of Module 2.4 and 2.6 eCTD submission documents.
  • Interpret and analyze applicable pharmacokinetics, pharmacology, and toxicology data (eg, Prism files, bioanalytical reports, clinical pathology reports, PK/TK evaluation reports).
  • Collaborate with cross-functional teams such as project management, safety, efficacy, biostats, regulatory operations, and CMC.
  • Demonstrated ability to lead others to complete complex projects.
  • Ability to complete documents according to sponsor’s format, processes, and according to regulatory guidelines.
  • Ability to effectively operate in an environment that requires negotiation, persuasion, collaboration, and analytical judgment.
  • Organizational expert within the nonclinical subject area.
  • Excellent written/oral communication and strong time and project management skills.
  • Ability to attend regular team meetings, lead client meeting and CRMs.
  • Ability to work in various client systems (eg, SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars.
  • Strong understanding of regulatory guidances as it applies to nonclinical submission documents and drug development (eg, ICH, FDA and EMA regulations and guidelines, GLP, GCP, GMP and GDP).

Requirements:

  • BS + in pharmacology, toxicology, biology or chemistry, or related field, with industry experience within regulatory writing, regulatory affairs, laboratory sciences, quality assurance/control.
  • Knowledge of GLP, ICH guidelines, and applicable regulatory requirements.
  • 5+ years of pharmaceutical regulatory nonclinical writing experience.
  • Strong writing and analytical skills.
  • Proficiency with MS Office applications.   
  • Hands-on experience with clinical trial and pharmaceutical development preferred.
  • Basic understanding of CROs and scientific & nonclinical data/terminology, & the drug development process.

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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