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Pharmacovigilance Analytics Jobs (NOW HIRING)

micro1 AI

Pharmacovigilance Expert

Yonkers, NY · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

micro1 AI

Pharmacovigilance Expert

Miami Gardens, FL · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

VENESCO LLC

Pharmacovigilance Physician

Frederick, MD · On-site

Pharmacovigilance Physician Venesco is seeking a Pharmacovigilance Physician to provide medical ... analyses, and regulatory safety reporting. Requirements: Duties and Responsibilities * Review and ...

micro1 AI

Pharmacovigilance Expert

Saint George, UT · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

micro1 AI

Pharmacovigilance Expert

Beaumont, TX · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

micro1 AI

Pharmacovigilance Expert

Carrollton, TX · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

micro1 AI

Pharmacovigilance Expert

Cedar Rapids, IA · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

micro1 AI

Pharmacovigilance Expert

Saint Louis, MO · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

micro1 AI

Pharmacovigilance Expert

Spokane Valley, WA · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

micro1 AI

Pharmacovigilance Expert

Plano, TX · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

micro1 AI

Pharmacovigilance Expert

Springfield, IL · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

micro1 AI

Pharmacovigilance Expert

Springfield, MA · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

micro1 AI

Pharmacovigilance Expert

El Paso, TX · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

micro1 AI

Pharmacovigilance Expert

Hollywood, FL · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

micro1 AI

Pharmacovigilance Expert

Peoria, AZ · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

micro1 AI

Pharmacovigilance Expert

Athens, GA · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

micro1 AI

Pharmacovigilance Expert

Cape Coral, FL · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

micro1 AI

Pharmacovigilance Expert

Independence, MO · Remote

$70 - $80/hr

Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis. Preferred Qualifications * 5+ years of pharmacovigilance or drug safety ...

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How much do pharmacovigilance analytics jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for pharmacovigilance analytics in the United States is $46.22, according to ZipRecruiter salary data. Most workers in this role earn between $26.92 and $55.29 per hour, depending on experience, location, and employer.

What is the difference between Pharmacovigilance Analytics vs Pharmacovigilance Specialist?

AspectPharmacovigilance AnalyticsPharmacovigilance Specialist
Required CredentialsDegree in life sciences, data analysis skills, certifications in pharmacovigilance or data analyticsDegree in pharmacy, life sciences, or healthcare; pharmacovigilance training or certification
Work EnvironmentData analysis teams, pharmacovigilance departments, often in pharmaceutical companies or CROsPharmacovigilance departments, clinical operations, regulatory teams
Employer & Industry UsageUsed in pharmaceutical companies, CROs, and analytics firms for data-driven safety monitoringUsed in pharma companies, hospitals, and regulatory agencies for safety reporting and compliance

Pharmacovigilance Analytics focuses on analyzing safety data, utilizing data science and statistical tools, while Pharmacovigilance Specialists handle case processing, safety reporting, and compliance. Both roles are essential in drug safety but differ in their core functions and skill sets.

What does a pharmacovigilance analyst do?

A pharmacovigilance analyst monitors and assesses the safety of pharmaceutical products by collecting, reviewing, and analyzing adverse drug reaction reports. They ensure compliance with regulatory requirements, often using specialized databases and tools, and contribute to risk management and safety reporting processes within pharmaceutical or healthcare organizations.

What is pharmacovigilance analytics?

Pharmacovigilance analytics involves analyzing data related to drug safety and adverse events to identify potential risks associated with medications. Professionals in this field use statistical tools and databases to monitor, assess, and report safety signals, supporting regulatory compliance and patient safety efforts.
More about Pharmacovigilance Analytics jobs

What cities are hiring for Pharmacovigilance Analytics jobs?

Cities with the most Pharmacovigilance Analytics job openings:

What states have the most Pharmacovigilance Analytics jobs?

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Pharmacovigilance Analytics jobs near you
Infographic showing various Pharmacovigilance Analytics job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 93% Full Time, 3% Part Time, and 3% Contract. Highlights an 78% Physical, 7% Hybrid, and 15% Remote job distribution, with an average salary of $96,145 per year, or $46.2 per hour.

Pharmacovigilance Expert

micro1 AI

Yonkers, NY • Remote

$70 - $80/hr

Part-time

Posted 16 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.

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