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Remote Vendor Risk Analyst Jobs in Boise, ID (NOW HIRING)

Pharmacovigilance Expert

Nampa, ID · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... benefit-risk conclusions in alignment with best practices. * Assess template and structural ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... benefit-risk conclusions in alignment with best practices. * Assess template and structural ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... benefit-risk conclusions in alignment with best practices. * Assess template and structural ...

Senior Ground Up Construction Project Manager

Boise, ID · Remote

$106K - $144K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Develop risk management plans and lead project teams through established work authorization ... Manage vendors to ensure full compliance with all project policies and procedures, including the ...

Senior Dam Safety Engineer - FERC IC

Boise, ID · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This position can be fully remote and the option for flexible working hours is available for the ... Lead or participate in Potential Failure Modes Analysis (PFMA) and Level 2 Risk Analysis (L2RA ...

... risk, and technology programs. Recruiting for this role ends on 12/31/2026. Work you'll do As a ... Analyzing processes, controls, and tools to identify opportunities for ServiceNow configuration and ...

... risk, and technology programs. Recruiting for this role ends on 12/31/2026. Work you'll do As a ... Analyzing processes, controls, and tools to identify opportunities for ServiceNow configuration and ...

Project Manager, High-Voltage

Boise, ID · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

In its 2025 analysis of solar independent power producers, S&P Global ranked Clēnera as a top ten ... This role owns cost, schedule, scope, quality, and risk for the HV build and commissioning phases ...

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Project Manager, High-Voltage

Boise, ID · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This role owns cost, schedule, scope, quality, and risk for the HV build and commissioning phases ... vendors, and internal stakeholders, ensuring systems are safe, compliant, utility-approved, and ...

New

Director of Finance

Boise, ID · Remote

$180K - $230K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

InfluxData is a remote-first company with a globally distributed workforce. For more information ... analyze cost drivers, drive optimization initiatives, manage cloud vendor contracts, and secure ...

R&D Tax Credit Manager

Boise, ID · On-site +1

$96K - $125K/yr

  • Medical

  • Retirement

  • PTO

Remote (U.S.) - Company Based in Boise, Idaho Employment Type: Full-Time Our Client is seeking an ... Analyze business activities to determine whether projects satisfy the requirements of Internal ...

SIU Investigator I

Boise, ID · On-site +1

$77K - $147K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

USAA roles may offer remote or hybrid flexibility for active-duty military spouses consistent with ... analyze claims, gather evidence, and make informed recommendations. You will play a key part in ...

New

Showing results 21-40

Remote Vendor Risk Analyst information

See Boise, ID salary details

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How much do remote vendor risk analyst jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for remote vendor risk analyst in Boise, ID is $38.53, according to ZipRecruiter salary data. Most workers in this role earn between $28.37 and $46.92 per hour, depending on experience, location, and employer.

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Pharmacovigilance Expert

micro1 AI

Nampa, ID • Remote

$70 - $80/hr

Part-time

Posted 12 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.