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Remote Senior Medical Writer Jobs in Michigan (NOW HIRING)

... senior decision-makers, and leading structured evaluations to close. This remote role welcomes ... Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment

... senior decision-makers, and leading structured evaluations to close. This remote role welcomes ... Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment

(Remote) Senior Software Engineer

Wyoming, MI ยท Remote

$111K - $146K/yr

Excellent analytical, problem-solving, and technical writing skills. * Demonstrated ability to ... Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment

(Remote) Senior Software Engineer

Wyoming, MI ยท Remote

$111K - $146K/yr

Excellent analytical, problem-solving, and technical writing skills. * Demonstrated ability to ... Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment

Senior Technical Writer (Remote)

Kalamazoo, MI ยท On-site +1

$86K - $132K/yr

Remote or Hybrid or Onsite Stryker is hiring a Senior Technical Writer to join our Technical ... Minimum of 2+ years of experience in technical writing within the medical device industry

New

Senior Technical Writer (Remote)

Portage, MI ยท On-site +1

$86K - $132K/yr

Remote or Hybrid or Onsite Stryker is hiring a Senior Technical Writer to join our Technical ... Minimum of 2+ years of experience in technical writing within the medical device industry

New

Senior SourcingManager (Remote)

Kalamazoo, MI ยท Remote

$153K - $255K/yr

Remote Asa Senior SourcingManager (Remote)you'llplay a pivotal role in driving innovation ... Experience working in a highly regulated industry, preferably within the Medical Device industry ...

New

Job Title Sr. Examiner, Homeowner Claims Multi-State - Remote Requisition Number R7899 Sr. Examiner ... Write and review repair estimates, evaluate contractor estimates, and determine appropriate claim ...

This is a remote position with a full benefits package. The Lead Attorney is responsible for ... Must be willing and able to write articles and make presentations to clients, trade associations

Sr Attorney

Flint, MI ยท Remote

This is a remote position with a full benefits package. The Lead Attorney is responsible for ... Must be willing and able to write articles and make presentations to clients, trade associations

This is a remote position with a full benefits package. The Lead Attorney is responsible for ... Must be willing and able to write articles and make presentations to clients, trade associations

This is a remote position with a full benefits package. The Supervising Attorney is responsible for ... Must be willing and able to write articles and make presentations to clients, trade associations

This is a remote position with a full benefits package. The Supervising Attorney is responsible for ... Must be willing and able to write articles and make presentations to clients, trade associations

This is a remote position with a full benefits package. The Supervising Attorney is responsible for ... Must be willing and able to write articles and make presentations to clients, trade associations

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Showing results 1-20

Remote Senior Medical Writer information

See Michigan salary details

$30.5K

$119.7K

$215.7K

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

As of Aug 28, 2026, the average yearly pay for remote senior medical writer in Michigan is $119,658.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,600.00 and $144,700.00 per year, depending on experience, location, and employer.

What is a remote senior medical writer?

Remote senior medical writers are experienced professionals who create, review, and edit scientific and medical documents for pharmaceutical, biotechnology, or healthcare organizations while working from a remote location. Their work includes regulatory documents, clinical study reports, manuscripts, and educational materials. They ensure complex medical information is communicated clearly and accurately for both professional and lay audiences, and often collaborate with scientists, physicians, and regulatory teams. Senior medical writers typically have advanced degrees in life sciences and several years of writing experience.

How does a remote senior medical writer typically collaborate with cross-functional teams while working off-site?

As a Remote Senior Medical Writer, you will regularly collaborate with medical, regulatory, and project management teams using virtual communication tools like video meetings, shared document platforms, and project management software. Clear and proactive communication is crucial, as you may need to bridge time zones and coordinate feedback from multiple stakeholders. While working remotely offers flexibility, it also requires strong organizational skills to manage deadlines and ensure your deliverables align with team objectives. Building strong relationships and maintaining transparency with your colleagues are key to ensuring smooth project progression and high-quality medical content.

What are the key skills and qualifications needed to thrive as a remote senior medical writer, and why are they important?

A Remote Senior Medical Writer needs advanced scientific or medical knowledge, strong writing skills, and typically a relevant degree (e.g., life sciences, pharmacy, or medicine) with proven experience in medical communications. Familiarity with reference management tools, document management systems, and publication guidelines (such as ICMJE or GPP) is crucial. Exceptional attention to detail, time management, and the ability to communicate complex information clearly are standout soft skills. These competencies ensure the accurate, compliant, and timely delivery of high-quality medical documents vital for regulatory submissions, publications, and healthcare communications.

What is the difference between Remote Senior Medical Writer vs Remote Medical Writer?

AspectRemote Senior Medical WriterRemote Medical Writer
CredentialsTypically requires advanced degrees (MD, PhD, PharmD) and experienceOften requires a relevant degree, such as life sciences or healthcare, with less experience needed
Work EnvironmentWorks independently or leads projects, often in a collaborative team settingSupports medical writing tasks under supervision, often in a team
Employer & Industry UsageUsed by pharmaceutical, biotech, and healthcare companies for complex documentationUsed across similar industries for standard medical content creation

The main difference between a Remote Senior Medical Writer and a Remote Medical Writer lies in experience, responsibilities, and credentials. Senior Medical Writers typically have advanced degrees and more experience, handling complex projects and leading teams. Medical Writers are often earlier in their careers, focusing on supporting documentation tasks under supervision. Both roles are vital in the healthcare and pharmaceutical industries, but the senior position involves greater expertise and leadership responsibilities.

What are the most commonly searched types of Senior Medical Writer jobs in Michigan?

The most popular types of Senior Medical Writer jobs in Michigan are:

What are popular job titles related to Remote Senior Medical Writer jobs in Michigan?

For Remote Senior Medical Writer jobs in Michigan, the most frequently searched job titles are:

What cities in Michigan are hiring for Remote Senior Medical Writer jobs?

Cities in Michigan with the most Remote Senior Medical Writer job openings:

Senior Medical Writer (Remote)

MMS Holdings Inc.

Canton, MI โ€ข On-site, Remote

Full-time

Re-posted 10 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