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Remote Pharmaceutical Writing Jobs in Michigan (NOW HIRING)

Cigna Healthcare

POSITION SUMMARY This role is responsible for managing pharmaceutical manufacturer relationships ... Superior verbal and written communication, analytical and organizational skills. Ability to ...

The Cigna Group

POSITION SUMMARY This role is responsible for managing pharmaceutical manufacturer relationships ... Superior verbal and written communication, analytical and organizational skills. Ability to ...

Viatris

$100K - $150K/yr

... pharmaceutical sales experience. * Proficiency in speaking, comprehending, reading and writing ... Remote

Viatris

$100K - $150K/yr

... pharmaceutical sales experience. * Proficiency in speaking, comprehending, reading and writing ... Remote

Float Health

Intake Specialist

Detroit, MI · Remote

$17.50 - $23.50/hr

You'll serve as a liaison between specialty pharmacies, nurses, and patients-leveraging technology ... Exceptional written and verbal communication, including the ability to digest and explain complex ...

Float Health

Intake Specialist

Dearborn, MI · On-site +1

$48K - $50K/yr

You'll serve as a liaison between specialty pharmacies, nurses, and patients-leveraging technology ... Exceptional written and verbal communication, including the ability to digest and explain complex ...

Float Health

Intake Specialist

Lansing, MI · On-site +1

$48K - $50K/yr

You'll serve as a liaison between specialty pharmacies, nurses, and patients-leveraging technology ... Exceptional written and verbal communication, including the ability to digest and explain complex ...

Float Health

Intake Specialist

Detroit, MI · On-site +1

$48K - $50K/yr

You'll serve as a liaison between specialty pharmacies, nurses, and patients-leveraging technology ... Exceptional written and verbal communication, including the ability to digest and explain complex ...

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All JobsPharmaceutical Writing JobsRemote Pharmaceutical Writing JobsRemote Pharmaceutical Writing Jobs in Michigan

Remote Pharmaceutical Writing information

What is remote pharmaceutical writing?

Remote pharmaceutical writing involves creating, editing, and reviewing scientific documents related to pharmaceuticals, such as clinical trial reports, regulatory submissions, and medical publications, while working from a location outside of a traditional office. These writers use their expertise in science and medicine to communicate complex information clearly and accurately for regulatory authorities, healthcare professionals, and the public. Remote roles offer flexibility and often require strong research, writing, and project management skills, in addition to familiarity with industry guidelines and standards.

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

To thrive as a Remote Pharmaceutical Writer, you typically need a strong background in life sciences or pharmacy, excellent writing skills, and familiarity with regulatory and medical terminology. Proficiency in using document management systems, referencing software, and adhering to formats like ICH guidelines or AMA style is common. Attention to detail, time management, and effective communication are vital soft skills for working independently and collaborating remotely with cross-functional teams. These skills ensure the creation of accurate, compliant, and clear scientific documents essential for regulatory submissions and medical communications.

What are some common challenges faced by remote pharmaceutical writers, and how can they be managed?

Remote pharmaceutical writers often encounter challenges such as collaborating across time zones, managing strict regulatory deadlines, and ensuring clear communication with cross-functional teams like medical, regulatory, and marketing. To address these issues, it's helpful to establish regular virtual check-ins, use collaborative project management tools, and maintain thorough documentation of project progress. Being proactive about clarifying expectations and seeking feedback also helps ensure accuracy and alignment with client or team objectives.

What are popular job titles related to Remote Pharmaceutical Writing jobs in Michigan?

For Remote Pharmaceutical Writing jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Remote Pharmaceutical Writing jobs in Michigan look for?

The top searched job categories for Remote Pharmaceutical Writing jobs in Michigan are:

What cities in Michigan are hiring for Remote Pharmaceutical Writing jobs?

Cities in Michigan with the most Remote Pharmaceutical Writing job openings:

Remote Pharmaceutical Writing jobs near you
Infographic showing various Remote Pharmaceutical Writing job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 22% Part Time, 1% Temporary, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Senior Medical Writer (Remote)

MMS Holdings Inc.

Canton, MI • On-site, Remote

Full-time

Re-posted 20 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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