ZipRecruiter

Log In

2

Remote Teen Scientific Writer Jobs in Michigan (NOW HIRING)

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 ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Detroit, MI · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

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 ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Lansing, MI · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Warren, MI · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

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 ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Dearborn, MI · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

BetterHelp

Licensed Psychologist - Remote

Detroit, MI · Remote

$650/wk

... teens. Requirements: * 3+ years of mental health counseling experience * Master's or Doctorate in ... Excellent written communication. * Must have professional liability insurance. * Reliable Internet ...

next page

Showing results 1-20

All JobsTeen Scientific Writer JobsRemote Teen Scientific Writer JobsRemote Teen Scientific Writer Jobs in Michigan

Remote Teen Scientific Writer information

What is a remote teen scientific writer?

A Remote Teen Scientific Writer is a young individual, typically a high school student, who creates scientific articles, reports, or content while working from home or another off-site location. These writers research scientific topics, explain concepts in an accessible way, and may contribute to blogs, magazines, or educational websites. The role helps teens develop research and communication skills, and it's a great opportunity for those interested in science and writing to gain experience and build a portfolio. Most remote positions offer flexible hours and are ideal for students balancing schoolwork and extracurricular activities.

What are the key skills and qualifications needed to thrive as a remote teen scientific writer?

To excel as a Remote Teen Scientific Writer, strong research abilities, clear scientific writing skills, and a solid understanding of scientific concepts—often demonstrated through coursework or extracurricular achievements—are essential. Familiarity with word processing software, reference management tools, and online collaboration platforms is typically required. Exceptional time management, self-motivation, and the ability to communicate complex ideas in an accessible way are crucial soft skills. These competencies enable writers to produce accurate, engaging scientific content while meeting deadlines and collaborating remotely.

What are some common challenges faced by remote teen scientific writers, and how can they overcome them?

Remote Teen Scientific Writers often encounter challenges such as managing time effectively between academic obligations and writing assignments, understanding complex scientific concepts, and ensuring their work meets professional editorial standards. To overcome these, it’s helpful to create a structured schedule, seek mentorship from experienced writers or scientists, and make use of online resources for research and writing guidance. Regular communication with editors and collaborating writers can also provide valuable feedback and keep projects on track, fostering both skill development and confidence.

What are the most commonly searched types of Teen Scientific Writer jobs in Michigan?

The most popular types of Teen Scientific Writer jobs in Michigan are:

What are popular job titles related to Remote Teen Scientific Writer jobs in Michigan?

For Remote Teen Scientific Writer jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Remote Teen Scientific Writer jobs in Michigan look for?

The top searched job categories for Remote Teen Scientific Writer jobs in Michigan are:

What cities in Michigan are hiring for Remote Teen Scientific Writer jobs?

Cities in Michigan with the most Remote Teen Scientific Writer job openings:

Remote Teen Scientific Writer jobs near you
Infographic showing various Remote Teen Scientific Writer job openings in Michigan as of August 2026, with employment types broken down into 77% Full Time, 16% Part Time, and 7% Contract. Highlights an 100% 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

Apply