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Psur Aggregate Report Jobs (NOW HIRING)

YO AI Labs

Pharmacovigilance Expert - Remote

Phoenix, AZ · Remote

$70 - $80/hr

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 ...

New

YO AI Labs

Pharmacovigilance Expert - Remote

Seattle, WA · Remote

$70 - $80/hr

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 ...

New

Neurocrine Biosciences, Inc.

Scientist, Safety

San Diego, CA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... hoc aggregate reports (eg, DSUR, IND Annual Report, PADER, PBRER, PSUR, etc.) and safety-related health authority requests in accordance with regulatory requirements * Participate in ...

Neurocrine Biosciences

Scientist, Safety

San Diego, CA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... hoc aggregate reports (eg, DSUR, IND Annual Report, PADER, PBRER, PSUR, etc.) and safety-related health authority requests in accordance with regulatory requirements * Participate in ...

SystImmune, Inc

Drug Safety Physician

Princeton, NJ · On-site

$150K - $250K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Experience with preparation of aggregate reports (e.g., DSUR, PSUR/PBRER, PADER) * Experience in preparation of responses to regulatory authorities; experience with regulatory filing and related ...

Systimmune

Drug Safety Physician

Princeton, NJ · On-site

$150K - $250K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Experience with preparation of aggregate reports (e.g., DSUR, PSUR/PBRER, PADER) * Experience in preparation of responses to regulatory authorities; experience with regulatory filing and related ...

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Showing results 21-40

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Psur Aggregate Report information

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How much do psur aggregate report jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for psur aggregate report in the United States is $18.34, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $19.23 per hour, depending on experience, location, and employer.

What is the difference between Psur Aggregate Report vs Psur Data Analyst?

AspectPsur Aggregate ReportPsur Data Analyst
Required CredentialsTypically no specific certifications, but familiarity with PSUR reporting standardsOften requires a degree in data analysis, healthcare, or related fields; certifications like CAP or PCAP are common
Work EnvironmentRegulatory or pharmaceutical settings, focusing on report compilationData analysis departments within pharma or healthcare companies, working with large datasets
Employer & Industry UsageUsed by regulatory agencies and pharmaceutical companies for safety reportingEmployed by pharma companies, CROs, or healthcare organizations for data interpretation

The Psur Aggregate Report focuses on compiling and submitting safety data summaries for regulatory review, while the Psur Data Analyst interprets and analyzes the underlying data to support safety assessments. Both roles are integral to pharmacovigilance but differ in scope and responsibilities.

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Psur Aggregate Report jobs near you
Infographic showing various Psur Aggregate Report job openings in the United States as of August 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 75% In-person, and 25% Remote job distribution, with an average salary of $38,150 per year, or $18.3 per hour.

Pharmacovigilance Expert - Remote

YO AI Labs

Los Angeles, CA • Remote

$70 - $80/hr

Full-time

Posted 2 days ago

New

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.