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Remote Scientific Communications Jobs in Michigan

... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... the scientific aspects of study protocols and reports. * Excellent communication (written and ...

Strong written and verbal communication skills with experience working cross-functionally. You may ... Benefit Summary This role is remote but if you live within 50 miles within Dearborn, MI, you will ...

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Remote Scientific Communications information

What is a remote scientific communications professional?

A Remote Scientific Communications job involves creating, editing, and presenting scientific information in a clear and engaging way, often for both expert and non-expert audiences. Professionals in this field work from home or other remote locations, collaborating with researchers, healthcare professionals, or companies to develop content such as research articles, presentations, reports, and marketing materials. The goal is to convey complex scientific concepts accurately and effectively, ensuring that the intended audience can understand and use the information. This role requires strong writing skills, a solid understanding of scientific topics, and the ability to translate technical data into accessible language.

What are the key skills and qualifications needed to thrive as a remote scientific communications professional?

To thrive as a Remote Scientific Communications professional, you need a strong background in science (often a degree in life sciences or related fields), excellent writing skills, and the ability to interpret complex data. Familiarity with tools like Microsoft Office, reference management software (e.g., EndNote), and content management systems is typically required, along with certifications such as AMWA or CMPP being advantageous. Outstanding organizational skills, attention to detail, and the ability to collaborate virtually are crucial soft skills for excelling in this role. These abilities ensure accurate, clear, and effective dissemination of scientific information to both specialist and non-specialist audiences, supporting research objectives and regulatory compliance.

How does a remote scientific communications professional typically collaborate with researchers and subject matter experts?

Remote scientific communications professionals regularly interact with researchers and subject matter experts using digital tools such as video conferencing, collaborative document platforms, and project management software. Although they work off-site, maintaining clear and proactive communication is essential to accurately interpret complex scientific data and ensure messaging aligns with project goals. Building strong virtual relationships, scheduling regular check-ins, and clarifying expectations are common practices to overcome the challenges of distance and time zones. This collaborative approach helps ensure content accuracy, timely delivery, and effective dissemination of scientific information.

What is the difference between Remote Scientific Communications vs Remote Medical Writing?

AspectRemote Scientific CommunicationsRemote Medical Writing
Required CredentialsScience or related degree, communication skillsScience or healthcare degree, writing expertise
Work EnvironmentCollaborative, often interdisciplinary teamsIndependent, project-focused
Employer & Industry UsagePharmaceutical, biotech, research organizationsPharmaceutical, medical device, healthcare companies
Common Search & ComparisonYesYes

Remote Scientific Communications involves creating and managing scientific content, often for diverse audiences, emphasizing communication skills. Remote Medical Writing focuses specifically on producing medical documents like clinical study reports and regulatory submissions. While both roles require scientific backgrounds, Remote Scientific Communications emphasizes broader communication strategies, whereas Remote Medical Writing is more specialized in medical documentation.

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

The most popular types of Scientific Communications jobs in Michigan are:

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

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

What cities in Michigan are hiring for Remote Scientific Communications jobs?

Cities in Michigan with the most Remote Scientific Communications job openings:

Lead Analyst, Clinical Data Sciences (Remote)

Stryker

Portage, MI • On-site, Remote

$124K - $207K/yr

Full-time

Posted 3 days ago

New


Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

134th of 499 rated machine equipment manufacturers


Job description

Work Flexibility: Remote or Hybrid or Onsite

Stryker is hiring a Lead Analyst, Clinical Data Sciences for our Instruments division. This is a U.S.-based remote position, with preference for candidates located in the Eastern or Central time zones.

Join Stryker Instruments in a role that sits at the intersection of clinical evidence, analytics, and business strategy. This position serves as a key connector between clinical questions and data-driven insights, helping stakeholders across Medical Affairs, Clinical Research, Regulatory Affairs, Reimbursement, Market Access, and commercial teams make informed decisions based on high-quality evidence. As part of a growing Clinical Data Sciences function, you will help establish scalable evidence-management capabilities while shaping how clinical evidence is evaluated and leveraged across the organization.

This role combines evidence strategy, evidence management, and insight generation, partnering closely with technical experts who build data products and automation solutions. The position offers broad exposure across Stryker Instruments' portfolio and supports initiatives that influence product, regulatory, clinical, and investment decisions.

What You Will Do

  • Lead implementation and management of evidence workflows, including systematic review processes, data extraction, quality control, reporting, and evidence repositories.

  • Build and scale evidence-management processes across multiple business units, transforming clinical and regulatory requirements into standardized, repeatable workflows.

  • Translate clinical, regulatory, reimbursement, and business questions into structured analyses and evidence-based recommendations.

  • Generate and interpret insights from clinical literature, real-world evidence, registries, claims data, and other scientific sources.

  • Partner with Medical Affairs, Clinical Research, Regulatory Affairs, Market Access, and business stakeholders to prioritize evidence needs and communicate findings.

  • Support clinical evaluation reports, post-market clinical follow-up activities, publications, scientific communications, and regulatory submissions through evidence synthesis and analytical support.

  • Evaluate clinical evidence across product portfolios, identify evidence gaps, and support prioritization of future evidence-generation investments.

  • Drive continuous improvement by partnering with technical teams to automate evidence workflows, enhance data solutions, and expand adoption of evidence-management tools.

What You Need

Required

  • Bachelor's degree in Life Sciences, Biomedical Engineering, Epidemiology, Health Economics and Outcomes Research (HEOR), Public Health, Data Science, or a related field.
  • Minimum 4 years of experience in clinical evidence, medical affairs analytics, HEOR, epidemiology, clinical research, or data science with clinical application.
  • Experience translating clinical, scientific, regulatory, or business questions into structured analyses and actionable insights.
  • Experience conducting clinical literature reviews, evidence synthesis, systematic reviews, or evidence-management activities.
  • Experience presenting analytical findings and evidence-based recommendations to non-technical stakeholders.

Preferred

  • Advanced degree (MS, MPH, PhD, or equivalent) in Life Sciences, Engineering, Epidemiology, Biostatistics, Public Health, Data Science, or related field.
  • Hands-on experience with DistillerSR, ReadCube, or similar evidence-management platforms.
  • Familiarity with medical device regulatory requirements, including FDA submissions, European Union Medical Device Regulation (EU MDR), Clinical Evaluation Reports (CERs), and Post-Market Clinical Follow-Up (PMCF) activities.
  • Experience with analytics and visualization tools such as Power BI, Tableau, R, Python, or SQL.
  • Experience working with real-world data sources, healthcare claims, registries, or observational datasets.

United States of America Pay Ranges:

  • USN: $95,700 - $159,500 USD Annual
  • US5: $100,500 - $167,500 USD Annual
  • US10: $105,300 - $175,500 USD Annual
  • US15: $110,100 - $183,400 USD Annual
  • US20: $114,800 - $191,400 USD Annual
  • US30: $124,400 - $207,400 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.

Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.

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