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Remote Development Writer Jobs in Michigan (NOW HIRING)

Wing Assistant

Sales Development Representative

Detroit, MI · On-site +1

$40K - $50K/yr

Confidence on the phone and in writing you can articulate value whether it's a 30-second cold call or a personalized email. * A reliable home/remote work setup and the self-discipline to run a high ...

Aptar Group

Business Development Manager

Midland, MI · On-site +1

Remote position; Preferably Midwest or East Coast in US (Western Europe possible) Travel: yes ... Excellent written and verbal communication skills, with the ability to articulate a compelling ...

micro1 AI

Lawyer - Remote

Dearborn, MI · Remote

$100 - $150/hr

... development. * Oversee the quality and accuracy of AI outputs, providing feedback to enhance ... Exceptional legal research, writing, and analytical abilities, with particular skill in issue ...

micro1 AI

Lawyer - Remote

Sterling Heights, MI · Remote

$100 - $150/hr

... development. * Oversee the quality and accuracy of AI outputs, providing feedback to enhance ... Exceptional legal research, writing, and analytical abilities, with particular skill in issue ...

micro1 AI

Lawyer - Remote

Grand Rapids, MI · Remote

$100 - $150/hr

... development. * Oversee the quality and accuracy of AI outputs, providing feedback to enhance ... Exceptional legal research, writing, and analytical abilities, with particular skill in issue ...

micro1 AI

Attorney - Remote

Lansing, MI · Remote

$100 - $150/hr

... development. * Oversee the quality and accuracy of AI outputs, providing feedback to enhance ... Exceptional legal research, writing, and analytical abilities, with particular skill in issue ...

micro1 AI

Attorney - Remote

Detroit, MI · Remote

$100 - $150/hr

... development. * Oversee the quality and accuracy of AI outputs, providing feedback to enhance ... Exceptional legal research, writing, and analytical abilities, with particular skill in issue ...

micro1 AI

Lawyer - Remote

Ann Arbor, MI · Remote

$100 - $150/hr

... development. * Oversee the quality and accuracy of AI outputs, providing feedback to enhance ... Exceptional legal research, writing, and analytical abilities, with particular skill in issue ...

micro1 AI

Attorney - Remote

Grand Rapids, MI · Remote

$100 - $150/hr

... development. * Oversee the quality and accuracy of AI outputs, providing feedback to enhance ... Exceptional legal research, writing, and analytical abilities, with particular skill in issue ...

micro1 AI

Lawyer - Remote

Lansing, MI · Remote

$100 - $150/hr

... development. * Oversee the quality and accuracy of AI outputs, providing feedback to enhance ... Exceptional legal research, writing, and analytical abilities, with particular skill in issue ...

micro1 AI

Attorney - Remote

Ann Arbor, MI · Remote

$100 - $150/hr

... development. * Oversee the quality and accuracy of AI outputs, providing feedback to enhance ... Exceptional legal research, writing, and analytical abilities, with particular skill in issue ...

micro1 AI

Attorney - Remote

Warren, MI · Remote

$100 - $150/hr

... development. * Oversee the quality and accuracy of AI outputs, providing feedback to enhance ... Exceptional legal research, writing, and analytical abilities, with particular skill in issue ...

micro1 AI

Lawyer - Remote

Warren, MI · Remote

$100 - $150/hr

... development. * Oversee the quality and accuracy of AI outputs, providing feedback to enhance ... Exceptional legal research, writing, and analytical abilities, with particular skill in issue ...

micro1 AI

Attorney - Remote

Dearborn, MI · Remote

$100 - $150/hr

... development. * Oversee the quality and accuracy of AI outputs, providing feedback to enhance ... Exceptional legal research, writing, and analytical abilities, with particular skill in issue ...

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All JobsDevelopment Writer JobsRemote Development Writer JobsRemote Development Writer Jobs in Michigan

Remote Development Writer information

What is the difference between Remote Development Writer vs Remote Content Writer?

AspectRemote Development WriterRemote Content Writer
Required CredentialsTechnical writing skills, familiarity with development topics, possibly coding knowledgeStrong writing skills, general research ability, SEO knowledge
Work EnvironmentTypically collaborates with developers, tech teams, and product managersWorks with marketing teams, editors, and content strategists
Employer & Industry UsageTech companies, software firms, development agenciesMedia outlets, marketing agencies, corporate blogs
Search & Comparison IntentUnderstanding technical writing roles in developmentExploring general content creation roles

Remote Development Writers focus on creating technical documentation, tutorials, and guides related to software development, requiring technical expertise. Remote Content Writers produce a broader range of content, including blogs, articles, and marketing materials, with less technical specialization. Both roles are remote, but their target industries and skill sets differ significantly.

What are the most commonly searched types of Development Writer jobs in Michigan? The most popular types of Development Writer jobs in Michigan are:
What cities in Michigan are hiring for Remote Development Writer jobs? Cities in Michigan with the most Remote Development Writer job openings:
Remote Development Writer jobs near you
Senior Medical Writer (Remote)

Senior Medical Writer (Remote)

MMS Holdings Inc.

Canton, MI • On-site, Remote

Full-time

Posted 26 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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