2

Remote Rn Case Review Jobs in Vancouver, WA (NOW HIRING)

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level ...

We provide a wellness and professional development stipend (up to $300 annually), case consultation ... Application Review: We'll promptly review your application to ensure you meet the minimum ...

We provide a wellness and professional development stipend (up to $300 annually), case consultation ... Application Review: We'll promptly review your application to ensure you meet the minimum ...

Remote micro1 is engaging Computational Biology Experts to contribute their advanced scientific ... Develop and review problem sets, case studies, or scenarios based on real-world medicinal chemistry ...

Showing results 41-60

Remote Rn Case Review information

See Vancouver, WA salary details

$20

$49

$83

How much do remote rn case review jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for remote rn case review in Vancouver, WA is $49.76, according to ZipRecruiter salary data. Most workers in this role earn between $37.02 and $60.14 per hour, depending on experience, location, and employer.

What is the difference between Remote Rn Case Review vs Remote Rn Utilization Review?

AspectRemote Rn Case ReviewRemote Rn Utilization Review
CredentialsRegistered Nurse (RN), licensure, case review certificationsRegistered Nurse (RN), licensure, utilization review certifications
Work EnvironmentRemote, healthcare settings, insurance companiesRemote, healthcare settings, insurance companies
Employer & IndustryHospitals, insurance firms, healthcare providersInsurance companies, healthcare management organizations

Remote Rn Case Review and Remote Rn Utilization Review roles both involve remote nursing work within the healthcare and insurance industries. While they share similar credentials and work environments, case review focuses on evaluating individual patient cases, whereas utilization review assesses the necessity and appropriateness of healthcare services. Understanding these distinctions helps job seekers identify the right role based on their skills and career goals.

Pharmacovigilance Expert

micro1 AI

Hillsboro, OR • Remote

$70 - $80/hr

Part-time

Posted 6 days ago


Job description

Role Title: Pharmacovigilance Expert


Role Type: Contractor


Location: Remote


micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. 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. This opportunity is ideal for professionals experienced in authoring and reviewing complex safety reports, passionate about data quality, and committed to clear written and verbal communication.


Scope of Work

  1. Author and review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level records.
  2. Apply expert judgment to assess the accuracy and adequacy of interval safety findings, signal evaluations, and benefit-risk conclusions in alignment with best practices.
  3. Assess template and structural conformity to ICH E2F and ICH E2C requirements, including proper section content, presentation of cumulative versus interval data, and completeness of appendices.
  4. Reconcile figures and case counts across report sections and data sources, identifying and documenting discrepancies significant for regulatory review.
  5. Evaluate safety conclusions in light of new data or events, and provide clear, structured written rationales supporting your determinations.
  6. Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis.


Preferred Qualifications

  1. 5+ years of pharmacovigilance or drug safety experience at a sponsor, CRO, or as an independent consultant.
  2. Demonstrated proficiency in authoring or reviewing DSURs and/or PSURs/PBRERs from start to finish.
  3. Working fluency with ICH E2F, ICH E2C(R2), and GVP guidelines, including signal management and benefit-risk assessment methodology.
  4. Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness determination, and aggregate safety data analysis.
  5. Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level information.
  6. Advanced degree in life sciences, pharmacy, nursing, or medicine (PharmD, MD, MSc, or equivalent).
  7. Experience in both development-stage and post-marketing safety reporting, QPPV or deputy QPPV roles, safety committee participation, or AI-assisted safety review tools is a plus.