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Remote Medical Review Officer Jobs in Indiana (NOW HIRING)

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

Medical Writing Manager

Carmel, IN · Remote

$50 - $80/hr

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

Coder - Clinic (remote)

Merrillville, IN · Remote

$18.50 - $24.50/hr

Remote availability Job Summary : Under general supervision and according to industry standards ... Performs charge entry, review, reconciliation, and error correction tasks to ensure full and ...

Coder - Clinic (remote)

Merrillville, IN · On-site +1

$20.89 - $33.43/hr

Remote availability Job Summary : Under general supervision and according to industry standards ... Performs charge entry, review, reconciliation, and error correction tasks to ensure full and ...

Showing results 21-40

Remote Medical Review Officer information

What is a remote medical review officer?

A Remote Medical Review Officer (MRO) is a licensed physician who is responsible for reviewing and interpreting drug test results in a remote or telework setting. They serve as an independent and impartial party to ensure the accuracy and integrity of drug testing processes, mainly for workplace drug screening programs. The MRO reviews laboratory results, interviews individuals regarding test results, and determines if there is a legitimate medical explanation for any positive findings. Working remotely, they utilize secure digital platforms to communicate with clients, laboratories, and employees while maintaining confidentiality and compliance with legal regulations.

What are the key skills and qualifications needed to thrive as a remote medical review officer, and why are they important?

To thrive as a Remote Medical Review Officer, you need a valid medical degree (MD or DO), licensure, and expertise in interpreting laboratory and toxicology results. Familiarity with secure telemedicine platforms, electronic health records (EHRs), and drug testing management software is essential. Strong attention to detail, ethical judgment, and effective written communication are standout soft skills in this role. These competencies are crucial for ensuring regulatory compliance, accurate decision-making, and trustworthy client interactions in remote settings.

How does a remote medical review officer typically collaborate with other healthcare professionals while working offsite?

As a Remote Medical Review Officer, you'll regularly collaborate with healthcare providers, laboratory staff, and case managers through secure digital communication channels, such as teleconferencing, email, and specialized electronic medical record systems. Although you're not onsite, effective teamwork is essential for reviewing test results, clarifying clinical information, and ensuring compliance with regulatory standards. You'll need strong communication skills to coordinate efficiently, resolve discrepancies, and provide clear, timely feedback to all stakeholders involved in the patient care process.

What is the difference between Remote Medical Review Officer vs Remote Drug and Alcohol Tester?

AspectRemote Medical Review OfficerRemote Drug and Alcohol Tester
CredentialsMedical license, certification in MRO or related fieldsCertification in drug testing or collection procedures
Work EnvironmentReviewing medical records remotely, analyzing drug test resultsConducting or overseeing drug and alcohol tests remotely or at collection sites
Industry UsageHealthcare, DOT compliance, occupational healthWorkplace safety, transportation, employment screening

The Remote Medical Review Officer primarily reviews medical records and drug test results to ensure compliance, requiring medical credentials. In contrast, Remote Drug and Alcohol Testers focus on administering or overseeing drug testing processes. Both roles are essential in workplace health and safety but differ in responsibilities and required qualifications.

What are the most commonly searched types of Medical Review Officer jobs in Indiana?

The most popular types of Medical Review Officer jobs in Indiana are:

What cities in Indiana are hiring for Remote Medical Review Officer jobs?

Cities in Indiana with the most Remote Medical Review Officer job openings:

Infographic showing various Remote Medical Review Officer job openings in Indiana as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% Remote job distribution.

Medical Writing Manager

micro1 AI

South Bend, IN • 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.