Pharmacovigilance Expert
Pharmacovigilance Expert is a current Micro1 opportunity with applicant compensation of $70 - $80/hour and explicit remote or location eligibility of Remote.
- Pay
- Firm hourly pay: $70 - $80/hour
- Location
- Remote
- Eligibility
- Remote, applicant location not specified
- Qualification difficulty
- Selective
How current is this information?
The public role and application path were checked. Details can still change; this is not an endorsement or guarantee.
- Platform
- Micro1
- Fit category
- Software engineering
- Listing/source checked
- Sep 12, 2026
- Apply link checked
- Sep 12, 2026
Application
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What this role involves
Pharmacovigilance Expert is a current Micro1 opportunity with applicant compensation of $70 - $80/hour and explicit remote or location eligibility of Remote.
What you’d do
- Author and review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level records.
- Apply expert judgment to assess the accuracy and adequacy of interval safety findings, signal evaluations, and benefit-risk conclusions in alignment with best practices.
- 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.
- Reconcile figures and case counts across report sections and data sources, identifying and documenting discrepancies significant for regulatory review.
- Evaluate safety conclusions in light of new data or events, and provide clear, structured written rationales supporting your determinations.
What they’re looking for
- 5+ years of pharmacovigilance or drug safety experience at a sponsor, CRO, or as an independent consultant.
Before you apply
Review the main fit signals and unresolved details before opening the platform.
Why it may fit
- Applicants whose experience directly matches the current Pharmacovigilance Expert qualifications.
- Professionals eligible for the stated Micro1 location and remote-work conditions: Remote.
Check before applying
Reasons to pause
- You cannot meet the public role's stated location or eligibility requirements.
- You need guaranteed acceptance, hours, pay, or project duration.
Still to verify
- Review the current Micro1 job post before applying. Role type, contractor status, location, screening steps, pay text, hours, and availability can change.
- Applicant eligibility still needs checking: Remote, applicant location not specified.
What to prepare
- 5+ years of pharmacovigilance or drug safety experience at a sponsor, CRO, or as an independent consultant. Demonstrated proficiency in authoring or reviewing DSURs and/or PSURs/PBRERs from start to finish. Working fluency with ICH E2F, ICH E2C(R2), and GVP guidelines, including signal management and benefit-risk assessment methodology. Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness determination, and aggregate safety data analysis. Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level information. Advanced degree in life sciences, pharmacy, nursing, or medicine (PharmD, MD, MSc, or equivalent). 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.
Role tools
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