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Real World Evidence Remote Jobs in Iowa (NOW HIRING)

micro1 AI

Medical Writing Manager

Cedar Rapids, IA · Remote

$50 - $80/hr

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Your work will shape how models learn, reason, and perform through high-quality, real-world input.

micro1 AI

Medical Billing Specialist

Cedar Rapids, IA · Remote

$50 - $80/hr

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Your work will shape how models learn, reason, and perform through high-quality, real-world input.

micro1 AI

Medical Billing Specialist

Davenport, IA · Remote

$50 - $80/hr

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Your work will shape how models learn, reason, and perform through high-quality, real-world input.

Accounting Fly

Remote Tax Senior

Cedar Rapids, IA · Remote

$80K - $100K/yr

Remote Tax Senior (Real Estate & Entrepreneurship) Job ID: 984010 Date Posted: July 28, 2026 ... Role Summary Are you a tax professional who enjoys the fast-paced world of entrepreneurs and real ...

Genpact

Sr. Associate - FCRM 5B

Guss, IA · Remote

Sr. Associate - FCRM Ready to turn bold ideas into real-world impact? At Genpact, we don't just ... Type - Remote Work Shift - Rotating (United States of America) The approximate annual base ...

Genpact

Sr. Associate - Customer Care - Voice 5B

Guss, IA · Remote

$19.25 - $26.25/hr

Sr. Associate - Customer Care - Voice Ready to turn bold ideas into real-world impact? At Genpact ... Type - Remote Work Shift - Rotating (United States of America) The approximate annual base ...

Genpact

Associate - BCM - Retirement 5A

Guss, IA · Remote

Associate - BCM - Retirement Ready to turn bold ideas into real-world impact? At Genpact, we don't ... Type - Remote Work Shift - Variable (United States of America) The approximate annual base ...

Genpact

Associate - Customer Care - Non - Voice 5A

Guss, IA · Remote

$14.50 - $20/hr

Associate - Customer Care - Non - Voice Ready to turn bold ideas into real-world impact? At Genpact ... Type - Remote Work Shift - Rotating (United States of America) The approximate annual base ...

Genpact

Analyst - Process Analytics - FCRM 5B

Guss, IA · Remote

Analyst - Process Analytics - FCRM Ready to turn bold ideas into real-world impact? At Genpact, we ... Remote Type - Remote Work Shift - Any (United States of America) The approximate annual base ...

Genpact

Associate - Customer Care - Voice 5A

Guss, IA · Remote

$14.50 - $20/hr

Associate - Customer Care - Voice Ready to turn bold ideas into real-world impact? At Genpact, we ... Type - Remote Work Shift - Rotating (United States of America) The approximate annual base ...

Genpact

Associate - Customer Care - Non - Voice 5A

Guss, IA · Remote

$14.50 - $20/hr

Associate - Customer Care - Non - Voice Ready to turn bold ideas into real-world impact? At Genpact ... Remote Type - Remote Work Shift - Any (United States of America) The approximate annual base ...

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Real World Evidence Remote information

What is a real world evidence (RWE) professional?

A Real World Evidence (RWE) professional is someone who collects, analyzes, and interprets data from real-life clinical settings to inform healthcare decisions. Unlike traditional clinical trials, RWE uses data from sources such as electronic health records, insurance claims, patient registries, and wearable devices. These professionals help pharmaceutical companies, regulatory agencies, and healthcare providers understand how treatments work in diverse, everyday populations. Their work supports drug development, regulatory submissions, and improved patient outcomes, often working remotely with data science and epidemiology teams.

What are the key skills and qualifications needed to thrive as a real world evidence (RWE) professional working remotely?

To thrive as a Real World Evidence professional, you need a strong background in epidemiology, data analysis, and life sciences, often supported by an advanced degree such as a Master's or PhD. Familiarity with statistical software (like SAS, R, or Python), data visualization tools, and experience working with large healthcare databases are typically required. Excellent communication, self-motivation, and organizational skills help remote RWE professionals collaborate effectively and manage projects independently. These skills ensure rigorous, high-impact research that informs healthcare decisions and supports regulatory submissions in a remote, data-driven environment.

What are the common challenges faced by professionals in remote real world evidence (RWE) roles and how can they be addressed?

One common challenge in remote RWE positions is effective collaboration with cross-functional teams, as these roles often require close coordination with clinical, data science, and regulatory colleagues across different time zones. Clear communication and proactive scheduling of virtual meetings are essential to stay aligned on project objectives. Additionally, remote RWE professionals must be adept at managing large, complex datasets securely from home, which requires a strong understanding of data privacy protocols and remote access tools. Regular training and leveraging secure, cloud-based platforms can help address these challenges and ensure productivity.
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Real World Evidence Remote jobs near you

Medical Writing Manager

micro1 AI

Cedar Rapids, IA • Remote

$50 - $80/hr

Part-time

Posted 5 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