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Remote Literary Jobs in Michigan (NOW HIRING)

State of Michigan

Evaluation Intern

Lansing, MI · On-site +1

$15.25 - $20.25/hr

Internship - Non Paid Remote Employment: Flexible/Hybrid Job Number: 4301-21-Workforce-Dev-Training ... Conduct literature reviews on evaluation methods and best practices. * Assist with survey ...

Amrize

Product Manager

Northville, MI · Remote

Building Envelope - Corp Northville, MI, Remote Worker - Michigan, Remote Worker - Michigan ABOUT ... Collaborate with Marketing to develop compelling product collateral, technical literature, and ...

Hurley Medical Center

Inpatient Coder - Fully Remote

Flint, MI · Remote

$21.50 - $25.75/hr

Enhances coding knowledge and skills with continuing education activities and by reviewing pertinent literature. * Knowledge of professional coding practices. * Ability to communicate effectively in ...

Viatris

$100K - $150K/yr

Leverage sample program, literature and other items to ensure physician awareness of Viatris ... Remote

Hurley Medical Center

Inpatient Coder - Fully Remote

Flint, MI · Remote

$21.25 - $25.50/hr

Enhances coding knowledge and skills with continuing education activities and by reviewing pertinent literature. * Knowledge of professional coding practices. * Ability to communicate effectively in ...

Viatris

$100K - $150K/yr

Leverage sample program, literature and other items to ensure physician awareness of Viatris ... Remote

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Remote Literary information

See Michigan salary details

$18.9K

$66.5K

$144.5K

How much do remote literary jobs pay per year?

As of Jul 28, 2026, the average yearly pay for remote literary in Michigan is $66,510.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,005.00 and $91,330.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Remote Literary position, and why are they important?

To thrive in a Remote Literary role, you should possess excellent reading comprehension, critical analysis, and written communication skills, often supported by a degree in literature, English, or a related field. Familiarity with digital communication platforms, manuscript editing software, and document collaboration tools is typically required. Strong self-motivation, time management, and the ability to work independently are key soft skills for remote success. These skills enable effective literary analysis, seamless remote collaboration, and high-quality project output in a distributed work environment.

What are the typical daily activities and team dynamics for someone in a Remote Literary position?

In a Remote Literary role, your typical day may involve reading and reviewing manuscripts, providing editorial feedback, conducting research, and collaborating with authors, editors, or publishing teams via online platforms. You’ll often participate in virtual meetings or communicate through email and project management tools to stay aligned with the broader team goals. While much of the work is done independently, success depends on clear communication and timely coordination with colleagues. Understanding these workflows allows you to manage your time efficiently and deliver consistent, high-quality literary contributions from a remote setting.

What is a Remote Literary job?

A Remote Literary job involves working in the literary field, such as writing, editing, publishing, or reviewing, from a remote location. These roles can include freelance or full-time positions in areas like book editing, manuscript evaluation, content writing, or literary agency work. Professionals in this field often collaborate with authors, publishers, or media companies to produce and refine written content. Strong communication, research, and editing skills are essential for success in remote literary jobs.

What are the most commonly searched types of Literary jobs in Michigan? The most popular types of Literary jobs in Michigan are:
What are popular job titles related to Remote Literary jobs in Michigan? For Remote Literary jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Remote Literary jobs in Michigan look for? The top searched job categories for Remote Literary jobs in Michigan are:
What cities in Michigan are hiring for Remote Literary jobs? Cities in Michigan with the most Remote Literary job openings:
Remote Literary jobs near you
Infographic showing various Remote Literary job openings in Michigan as of July 2026, with employment types broken down into 11% As Needed, 23% Full Time, 59% Part Time, and 7% Nights. Highlights an 14% Physical, and 86% Remote job distribution, with an average salary of $66,510 per year, or $32 per hour.
Senior Medical Writer (Remote)

Senior Medical Writer (Remote)

MMS Holdings Inc.

Canton, MI • On-site, Remote

Full-time

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

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