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Remote Medical Scientist Jobs in Park Ridge, IL (NOW HIRING)

Tempus

Scientist II, Translational Research

Chicago, IL · On-site +1

$100K - $150K/yr

... Science teams. Work with Product and Engineering teams to streamline workflow of computational ... medical and other benefits depending on the position. Additionally, for remote roles open to ...

YO AI Labs

Clinical Document Author - Remote

Chicago, IL · Remote

$50 - $80/hr

Remote Job Type: Contractor Pay: $50-$80/hour Job Overview We are seeking an experienced Medical ... Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific ...

Danaher

Inside Sales Representative (REMOTE)

Chicago, IL · On-site +1

$33.65 - $43.27/hr

We bring together deep scientific expertise, an unwavering commitment to quality, and a ... We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance ...

Danaher

Inside Sales Representative (REMOTE)

Chicago, IL · On-site +1

$33.65 - $43.27/hr

We bring together deep scientific expertise, an unwavering commitment to quality, and a ... We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance ...

Enara Health

Remote Nutrition Specialist

Chicago, IL · Remote

$26 - $36/hr

About Enara Enara is a world renowned obesity and medical weight loss start-up, based in Silicon ... Our platform allows for the latest breakthroughs in nutrition, exercise, and obesity science to be ...

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Showing results 41-60

All JobsMedical Scientist JobsRemote Medical Scientist JobsRemote Medical Scientist Jobs in Park Ridge, IL

Remote Medical Scientist information

See Park Ridge, IL salary details

$37.9K

$60.7K

$97.9K

How much do remote medical scientist jobs pay per year?

As of Aug 22, 2026, the average yearly pay for remote medical scientist in Park Ridge, IL is $60,677.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,300.00 and $72,300.00 per year, depending on experience, location, and employer.

What is the difference between Remote Medical Scientist vs Remote Clinical Research Associate?

AspectRemote Medical ScientistRemote Clinical Research Associate
Required CredentialsAdvanced degree in life sciences, often PhD or Master'sBachelor's or Master's in life sciences or related field
Work EnvironmentResearch labs, pharmaceutical companies, or remote settingsClinical trial sites, monitoring, and remote oversight
Employer & Industry UsagePharmaceutical, biotech, research institutionsClinical trial organizations, CROs, pharmaceutical companies
Common Search & ComparisonYesYes

Remote Medical Scientists focus on designing and analyzing research studies, often requiring advanced degrees. Remote Clinical Research Associates primarily monitor clinical trials and ensure compliance. Both roles are integral to medical research but differ in responsibilities and qualifications.

Are remote medical scientists in high demand?

Remote medical scientists are in increasing demand due to advancements in telehealth, data analysis, and research technology. The role often requires strong analytical skills, knowledge of laboratory procedures, and relevant certifications, with employment opportunities growing in both academic and industry settings.

What cities near Park Ridge, IL are hiring for Remote Medical Scientist jobs?

Cities near Park Ridge, IL with the most Remote Medical Scientist job openings:

Remote Medical Scientist jobs near you

Medical Writer / Clinical Document Author

micro1 AI

Chicago, IL • Remote

$50 - $80/hr

Part-time

Posted 18 days ago

Job description

Role Title: Medical Writer / Clinical Document Author


Role Type: Contractor


Location: Remote


micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer’s project focused on developing advanced AI-assisted writing tools for clinical documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  2. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  3. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  4. Trace narrative claims to source records—tables, figures, listings, and protocols—to verify that all assertions are appropriately supported.
  5. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  6. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.


Preferred Qualifications

  1. Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  2. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  3. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  4. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  5. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  6. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  7. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.


Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents — through your expert input, judgment, and real-world experience.

Apply