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Weekend Pharmacovigilance Jobs (NOW HIRING)

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 ...

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 ...

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 ...

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 ...

Pharmacovigilance Expert

Plano, TX · Remote

$70 - $80/hr

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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Weekend Pharmacovigilance information

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$12

$49

$85

How much do weekend pharmacovigilance jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for weekend 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 is a weekend pharmacovigilance?

Weekend Pharmacovigilance jobs involve monitoring, assessing, and reporting on the safety of pharmaceutical products during weekends. Professionals in these roles review adverse event reports, ensure compliance with regulatory requirements, and may respond to urgent safety issues outside of regular business hours. These positions are crucial for maintaining continuous drug safety surveillance and supporting healthcare providers and patients at all times, including weekends.

What are the typical responsibilities and workflow for a weekend pharmacovigilance professional?

Weekend Pharmacovigilance professionals are primarily responsible for monitoring, assessing, and reporting adverse drug reactions and safety issues that arise during their shifts. Their workflow often involves triaging urgent safety cases, entering and validating case data, and collaborating with other team members to ensure timely regulatory submissions. Since much of the work occurs outside standard hours, strong communication with weekday teams is essential for seamless case handover and continuity. Additionally, they may participate in safety surveillance meetings or support ongoing investigations, making adaptability and attention to detail crucial in this role.

What are the key skills and qualifications needed to thrive as a weekend pharmacovigilance professional, and why are they important?

To thrive as a Weekend Pharmacovigilance professional, you need a solid background in pharmacy, life sciences, or healthcare, often with a relevant degree and experience in drug safety or regulatory affairs. Familiarity with pharmacovigilance databases (such as Argus or ARISg), adverse event reporting systems, and knowledge of regulatory guidelines like ICH and FDA are typically required. Strong attention to detail, effective communication, and time management are important soft skills for handling urgent reports and collaborating remotely. These skills ensure timely and accurate monitoring of drug safety, compliance with regulations, and protection of patient well-being, even outside standard business hours.

What is the difference between Weekend Pharmacovigilance vs Pharmacovigilance Associate?

AspectWeekend PharmacovigilancePharmacovigilance Associate
CertificationsTypically requires a degree in pharmacy, life sciences, or related field; certifications like PV training are commonSame as Weekend Pharmacovigilance, often requiring similar educational background and certifications
Work EnvironmentPart-time, weekend shifts, often in pharmaceutical or biotech companiesFull-time or part-time, in clinical research organizations or pharmaceutical companies
Industry UsageUsed in companies needing weekend safety monitoring coverageCommon entry-level role in pharmacovigilance teams

Weekend Pharmacovigilance and Pharmacovigilance Associate roles share similar educational requirements and industry settings. The main difference lies in the work schedule, with Weekend Pharmacovigilance focusing on weekend shifts, while Pharmacovigilance Associates typically work full-time during weekdays. Both roles are essential for ensuring drug safety and require comparable qualifications.

More about Weekend Pharmacovigilance jobs

What cities are hiring for Weekend Pharmacovigilance jobs?

Cities with the most Weekend Pharmacovigilance job openings:

What are the most commonly searched types of Pharmacovigilance jobs?

The most popular types of Pharmacovigilance jobs are:

What states have the most Weekend Pharmacovigilance jobs?

States with the most job openings for Weekend Pharmacovigilance jobs include:

Infographic showing various Weekend Pharmacovigilance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 26% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

Pharmacovigilance Expert

micro1 AI

Miami Gardens, FL • 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.