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Remote Science Consulting Jobs in Michigan (NOW HIRING)

Stefanini Group

Epic Data Engineer

Grand Rapids, MI · Remote

Stefanini is looking for Epic Data Engineer-Remote For quick apply, please contact Sudhanshu ... scientists to build and maintain analytic solutions utilizing both traditional on-premises and ...

Stefanini Group

Epic Data Engineer

Grand Rapids, MI · Remote

Stefanini is looking for Epic Data Engineer-Remote For quick apply, please contact Sudhanshu ... scientists to build and maintain analytic solutions utilizing both traditional on-premises and ...

Stefanini Group

Epic Data Engineer

Grand Rapids, MI · Remote

Stefanini is looking for Epic Data Engineer-Remote For quick apply, please contact Sudhanshu ... scientists to build and maintain analytic solutions utilizing both traditional on-premises and ...

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Remote Science Consulting information

What are some common challenges faced by remote science consultants, and how can they be addressed?

Remote science consultants often encounter challenges related to communication and collaboration, especially when working with clients or teams across different time zones. Establishing clear communication protocols, using collaboration tools, and scheduling regular check-ins can help mitigate misunderstandings and keep projects on track. Additionally, maintaining a structured work routine and creating a dedicated workspace can improve productivity and work-life balance. Building strong client relationships remotely may require extra effort, such as proactive updates and transparent reporting.

What is remote science consulting?

Remote science consulting involves providing expert scientific advice, analysis, or services to organizations, businesses, or individuals from a distance, typically using digital communication tools. Consultants may help with research design, data analysis, regulatory compliance, or scientific writing without being physically present at the client’s location. This flexible arrangement allows clients to access specialized expertise regardless of geographic location, and consultants to work with a wider range of clients. Common fields include environmental science, pharmaceuticals, biotechnology, and data science.

What are the key skills and qualifications needed to thrive as a Remote Science Consultant, and why are they important?

To thrive as a Remote Science Consultant, you need a strong background in scientific research, data analysis, and domain-specific expertise, usually supported by an advanced degree in a relevant field. Proficiency with collaborative tools (like Slack or Zoom), data analysis software (such as R, Python, or MATLAB), and project management systems is typically required. Outstanding communication, self-motivation, and problem-solving skills help you effectively engage with clients and deliver solutions remotely. These skills and tools are essential for providing high-quality, evidence-based advice while maintaining productivity and trust in a remote work environment.
What are popular job titles related to Remote Science Consulting jobs in Michigan? For Remote Science Consulting jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Remote Science Consulting jobs in Michigan look for? The top searched job categories for Remote Science Consulting jobs in Michigan are:
What cities in Michigan are hiring for Remote Science Consulting jobs? Cities in Michigan with the most Remote Science Consulting job openings:
Remote Science Consulting jobs near you
Infographic showing various Remote Science Consulting job openings in Michigan as of July 2026, with employment types broken down into 76% Full Time, and 24% Part Time. Highlights an 100% Remote job distribution.
Senior Medical Writer (Remote)

Senior Medical Writer (Remote)

MMS Holdings Inc.

Canton, MI • On-site, Remote

Full-time

Re-posted 9 hours 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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