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Aggregate In Pharmacovigilance Jobs (NOW HIRING)

YO AI Labs

Pharmacovigilance Expert - Remote

Seattle, WA · Remote

$70 - $80/hr

Pharmacovigilance Expert Job Type: Contractor Location: Remote Job Overview We are seeking ... Experience reconciling aggregate safety data with case-level information. * Advanced degree in life ...

YO AI Labs

Pharmacovigilance Expert - Remote

Austin, TX · Remote

$70 - $80/hr

Pharmacovigilance Expert Job Type: Contractor Location: Remote Job Overview We are seeking ... Experience reconciling aggregate safety data with case-level information. * Advanced degree in life ...

YO AI Labs

Pharmacovigilance Expert - Remote

Boston, MA · Remote

$70 - $80/hr

Pharmacovigilance Expert Job Type: Contractor Location: Remote Job Overview We are seeking ... Experience reconciling aggregate safety data with case-level information. * Advanced degree in life ...

YO AI Labs

Pharmacovigilance Expert - Remote

Houston, TX · Remote

$70 - $80/hr

Pharmacovigilance Expert Job Type: Contractor Location: Remote Job Overview We are seeking ... Experience reconciling aggregate safety data with case-level information. * Advanced degree in life ...

YO AI Labs

Pharmacovigilance Expert - Remote

Miami, FL · Remote

$70 - $80/hr

Pharmacovigilance Expert Job Type: Contractor Location: Remote Job Overview We are seeking ... Experience reconciling aggregate safety data with case-level information. * Advanced degree in life ...

Med Communications

Pharmacovigilance Physician

... in the evaluation and interpretation of safety data for pharmaceutical products. This role is ... Evaluate aggregate safety information for periodic safety reports and ad hoc requests. * Support ...

micro1 AI

Pharmacovigilance Expert

Cincinnati, OH · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging ... Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level ...

micro1 AI

Pharmacovigilance Expert

Providence, RI · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging ... Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level ...

micro1 AI

Pharmacovigilance Expert

Greensboro, NC · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging ... Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level ...

micro1 AI

Pharmacovigilance Expert

Oklahoma City, OK · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging ... Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level ...

micro1 AI

Pharmacovigilance Expert

Surprise, AZ · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging ... Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level ...

micro1 AI

Pharmacovigilance Expert

Fayetteville, AR · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging ... Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level ...

micro1 AI

Pharmacovigilance Expert

Federal Way, WA · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging ... Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level ...

micro1 AI

Pharmacovigilance Expert

Irving, TX · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging ... Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level ...

micro1 AI

Pharmacovigilance Expert

Honolulu, HI · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging ... Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level ...

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Aggregate In Pharmacovigilance information

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$12

$49

$85

How much do aggregate in pharmacovigilance jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for aggregate in pharmacovigilance in the United States is $49.14, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $55.53 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an aggregate in pharmacovigilance?

To thrive in an Aggregate role in Pharmacovigilance, you need a solid background in life sciences or pharmacy, strong analytical abilities, and experience with safety data analysis and regulatory reporting. Familiarity with pharmacovigilance databases (such as Argus or ArisG), signal detection tools, and an understanding of global regulatory guidelines (e.g., ICH, EMA, FDA) are typically required. Excellent attention to detail, organizational skills, and effective communication are essential soft skills for interpreting complex data and collaborating across teams. These competencies are crucial for ensuring accurate safety reporting, regulatory compliance, and the protection of patient health.

What are some common challenges faced by professionals working in aggregate reporting within pharmacovigilance?

Professionals involved in aggregate reporting in pharmacovigilance often encounter challenges such as managing large volumes of data from multiple sources, ensuring compliance with evolving global regulatory requirements, and meeting strict submission deadlines. Coordinating with cross-functional teams—such as clinical, regulatory, and safety departments—is essential for gathering accurate information and maintaining data consistency. Attention to detail and strong organizational skills are crucial to ensure that periodic safety update reports (PSURs), periodic benefit-risk evaluation reports (PBRERs), and other aggregate reports are comprehensive and error-free.

What is the difference between Aggregate In Pharmacovigilance vs Pharmacovigilance Associate?

AspectAggregate In PharmacovigilancePharmacovigilance Associate
CredentialsTypically requires a degree in life sciences, pharmacy, or related field; certifications like PV training are commonSimilar educational background; often requires PV-specific training or certifications
Work EnvironmentFocuses on data analysis, signal detection, and reporting of safety data at a higher levelInvolves data entry, case processing, and supporting safety reports
Employer & Industry UsageUsed in pharmaceutical companies, CROs, and regulatory agencies for safety data analysisCommonly employed in similar settings for case management and data entry

In summary, Aggregate In Pharmacovigilance primarily handles data analysis and safety signal detection, requiring advanced skills in data interpretation. Pharmacovigilance Associates focus on case processing and data entry tasks. Both roles require relevant certifications and work within the same industry environment, but differ in scope and responsibilities.

What is aggregate reporting in pharmacovigilance?

In pharmacovigilance, aggregate reporting involves compiling and analyzing safety data from multiple individual adverse event reports over a specific period to identify safety signals and trends. Pharmacovigilance professionals use tools like safety databases and statistical methods to prepare periodic safety update reports (PSURs) and aggregate reports required by regulatory authorities.
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Aggregate In Pharmacovigilance jobs near you
Infographic showing various Aggregate In Pharmacovigilance job openings in the United States as of August 2026, with employment types broken down into 84% Full Time, 14% Part Time, 1% Contract, and 1% Nights. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

Pharmacovigilance Expert - Remote

YO AI Labs

Seattle, WA • Remote

$70 - $80/hr

Full-time

Posted 9 days ago

Job description

Job Title: Pharmacovigilance Expert

Job Type: Contractor
Location: Remote

Job Overview

We are seeking experienced Pharmacovigilance Experts to contribute their drug safety expertise to an innovative healthcare AI project. In this role, you will help improve next-generation AI systems by reviewing, evaluating, and refining pharmacovigilance documentation, safety reports, and regulatory content. No prior AI experience is required—your pharmacovigilance expertise, analytical skills, and commitment to data quality are what matter most.

Key Responsibilities

  • Author and review evaluation tasks based on DSURs, PSURs/PBRERs, safety data, and case-level records.

  • Assess safety findings, signal evaluations, and benefit-risk conclusions for accuracy and regulatory alignment.

  • Review reports for compliance with ICH E2F, ICH E2C(R2), and GVP guidelines.

  • Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources.

  • Evaluate safety conclusions based on new data, events, and regulatory requirements.

  • Provide structured written feedback and rationales to support AI-driven pharmacovigilance tools.

  • Ensure accuracy, completeness, and quality of regulatory safety documentation.

Required Skills

  • Pharmacovigilance

  • Drug Safety Report Authoring

  • DSUR/PSUR/PBRER Review

  • ICH E2F & ICH E2C(R2) Compliance

  • GVP Guidelines

  • Aggregate Safety Data Analysis

  • Signal Management

  • Benefit-Risk Assessment

  • MedDRA Coding

  • Seriousness & Causality Assessment

  • Expectedness Determination

  • Data Reconciliation

  • Regulatory Documentation

  • Structured Written Communication

  • Attention to Detail

Preferred Qualifications

  • 5+ years of pharmacovigilance or drug safety experience within a sponsor, CRO, or consulting environment.

  • Proven experience authoring or reviewing DSURs and/or PSURs/PBRERs.

  • Strong knowledge of ICH E2F, ICH E2C(R2), and GVP guidelines.

  • Hands-on experience with signal management, benefit-risk assessment, MedDRA coding, and safety data analysis.

  • Experience reconciling aggregate safety data with case-level information.

  • Advanced degree in life sciences, pharmacy, nursing, medicine, or related fields (PharmD, MD, MSc, or equivalent).

  • Experience in clinical development safety, post-marketing surveillance, QPPV/deputy QPPV roles, safety committees, or AI-assisted safety review tools is a plus.