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Clinical Writer Jobs in Michigan (NOW HIRING)

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

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

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

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

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

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

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

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 ...

micro1 AI

Medical Writing Manager

Sterling Heights, 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 ...

micro1 AI

Medical Writing Manager

Sterling Heights, 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

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 ...

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 ...

Hanger, Inc.

Clinical Assistant

Kalamazoo, MI

The Clinical Aide provides direct support to certified clinicians in delivering orthotic and ... Ability to follow written and verbal directions. * Hand skills necessary to use laboratory tools ...

Hospice of Michigan

Clinical Director

Ada, MI · On-site

$78K - $106K/yr

Clinical Director Job Summary: The Clinical Director, Service Operations is responsible for ... Must be able to read, write and speak English fluently and be able to communicate orally and in ...

Hanger, Inc.

Clinical Assistant

Kalamazoo, MI · On-site

The Clinical Aide provides direct support to certified clinicians in delivering orthotic and ... Ability to follow written and verbal directions. * Hand skills necessary to use laboratory tools ...

Hospice of Michigan

Clinical Director

Ada, MI · On-site

$78K - $106K/yr

Clinical Director Job Summary: The Clinical Director, Service Operations is responsible for ... Must be able to read, write and speak English fluently and be able to communicate orally and in ...

NEW PATHS INC

Clinical Tech

Flint, MI · On-site

$18.50 - $23.75/hr

Clinical Technician We are looking for Clinical Technicians to work 2nd or 3rd shift. Our mission ... Communicate shift report both verbally and in writing to coworkers each and every shift.

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Showing results 21-40

All JobsClinical Writer JobsClinical Writer Jobs in Michigan

Clinical Writer information

See Michigan salary details

$21

$47

$72

How much do clinical writer jobs pay per hour?

As of Aug 13, 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 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.

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 knowledge in regulatory writing or medical sciences.

How can I get into clinical writing with no experience?

Clinical writers create scientific documents for healthcare and pharmaceutical industries. To enter the field with no experience, gaining knowledge of medical terminology, regulatory guidelines, and writing skills through online courses or certifications can be helpful. Building a portfolio with sample documents and seeking entry-level or freelance opportunities can also improve chances of breaking into clinical writing.

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 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.
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 2% As Needed, 73% Full Time, 16% Part Time, 1% Temporary, and 8% Contract. 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.

Medical Writing Manager

micro1 AI

Ann Arbor, MI • Remote

$50 - $80/hr

Part-time

This job post has expired today. Applications are no longer accepted.

Job description

Role Title: 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 developing advanced AI-assisted writing tools for clinical documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  2. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  3. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  4. Trace narrative claims to source records—tables, figures, listings, and protocols—to verify that all assertions are appropriately supported.
  5. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  6. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.


Preferred Qualifications

  1. Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  2. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  3. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  4. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  5. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  6. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  7. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.


Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents — through your expert input, judgment, and real-world experience.

Apply