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Remote Pharmacovigilance Jobs in Reston, VA (NOW HIRING)

Pharmacovigilance Expert

Alexandria, VA ยท Remote

$70 - $80/hr

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 ...

Pharmacovigilance Expert

Washington, DC ยท Remote

$70 - $80/hr

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 ...

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 ...

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 ...

Overview Safety Manager US Remote Emmes Group: Building a better future for us all. Emmes Group is ... Primary Purpose The TA Safety Manager will implement Pharmacovigilance and Medical Monitoring (PMM ...

Clinicia Expert - Remote

Washington, DC ยท Remote

$150 - $200/hr

Remote Job Overview We are seeking experienced Clinicians specializing in Oncology and Hematology to contribute their medical expertise to an innovative healthcare AI project. In this role, you will ...

Remote arrangements can also be considered. Otsuka maintains a hybrid work policy and travel is ... Partner closely with Clinical Development, Clinical Pharmacology, Clinical Management, Regulatory ...

OP Coder

Washington, DC ยท On-site +1

$20.50 - $27.50/hr

Remote VA Experienced Outpatient Medical Coders Summary Cooper Thomas, LLC, a leading provider of ... processes, pharmacology, health record format and content, reimbursement methodologies and ...

This position is 100% remote. Essential Job Functions: * Applying appropriate FOIA exemptions to ... Nursing Pharmacology, etc.) or related field Required Experience: * Minimum three (3) years ...

Inpatient PTF Coders

Washington, DC ยท Remote

$22.25 - $26.75/hr

VA Experienced Remote Inpatient Facility Fee (PTF) Medical Coders-Full-Time Positions Available ... processes, pharmacology, health record format and content, reimbursement methodologies and ...

Inpatient PTF Coders

Washington, DC ยท On-site +1

$23.75 - $28.75/hr

VA Experienced Remote Inpatient Facility Fee (PTF) Medical Coders-Full-Time Positions Available ... processes, pharmacology, health record format and content, reimbursement methodologies and ...

Overview Project Leader - Biostatistician US Remote Emmes Group: Building a better future for us ... and Pharmacovigilance. * Perform statistical duties per statistical JDs level/experience and ...

Overview Senior Project Leader US Remote Emmes Group: Building a better future for us all. Emmes ... Pharmacovigilance. * Proactively assesses client expectations and addresses client's needs for ...

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Remote Pharmacovigilance information

See Reston, VA salary details

$23

$48

$87

How much do remote pharmacovigilance jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for remote pharmacovigilance in Reston, VA is $48.09, according to ZipRecruiter salary data. Most workers in this role earn between $28.03 and $57.50 per hour, depending on experience, location, and employer.

What is remote pharmacovigilance?

Remote pharmacovigilance refers to the practice of monitoring, assessing, and reporting the safety of pharmaceutical products from a remote location, often outside of a traditional office or clinical setting. Pharmacovigilance professionals in remote roles use digital tools and secure databases to collect and analyze data on adverse drug reactions and ensure compliance with regulatory requirements. This setup allows for flexibility and can increase efficiency while maintaining the integrity and confidentiality of sensitive patient and product data.

What are remote pharmacovigilance jobs?

Remote pharmacovigilance jobs include positions like pharmacovigilance scientist and risk management specialist. In these work from home jobs, you may research medical literature to look for potential adverse effects from pharmaceutical products, promote drug safety, help prevent the misuse of experimental compounds, and research the best ways to address an overdose of a given medication. Remote pharmacovigilance jobs focus heavily on research duties as well as helping provide strategic leadership when preparing regulatory submissions for new products or formulations. Many pharmacovigilance positions involve leading a team or working with other analysts to evaluate a certain medication or medical device.

What are the key skills and qualifications needed to thrive as a remote pharmacovigilance professional?

To excel in remote pharmacovigilance, you need a solid background in pharmacy, life sciences, or a related field, along with a good understanding of drug safety regulations and adverse event reporting. Familiarity with pharmacovigilance databases (such as Argus, ArisG), MedDRA coding, and relevant regulatory frameworks (like FDA or EMA guidelines) is crucial. Strong attention to detail, analytical thinking, and effective written communication are valuable soft skills for this role. These competencies ensure accurate safety data reporting, regulatory compliance, and effective collaboration in a virtual environment.

How does working remotely in pharmacovigilance impact collaboration with global teams and regulatory authorities?

Remote pharmacovigilance professionals often work with colleagues and stakeholders across multiple time zones, which requires strong communication and organizational skills. Regular virtual meetings, shared documentation platforms, and standardized reporting tools are commonly used to ensure seamless information exchange and compliance with regulatory requirements. While remote work offers flexibility, it also demands proactive engagement to stay aligned with team objectives and maintain timely responses to safety concerns. Successful remote pharmacovigilance specialists are adept at building relationships and collaborating effectively in a virtual environment.

What is the difference between Remote Pharmacovigilance vs Remote Drug Safety Associate?

AspectRemote PharmacovigilanceRemote Drug Safety Associate
CredentialsTypically requires pharmacovigilance certifications, life sciences degreeOften requires similar life sciences background, some certifications preferred
Work EnvironmentRemote, industry-focused, regulatory complianceRemote, clinical safety monitoring, data entry
Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, healthcare organizations

Remote Pharmacovigilance and Remote Drug Safety Associate roles share similar credentials and work environments, both focusing on drug safety in the pharmaceutical industry. However, pharmacovigilance often involves more regulatory compliance and adverse event analysis, while drug safety associates may focus more on data entry and case processing. Both roles are essential for ensuring medication safety and are commonly sought in remote healthcare jobs.

What are the most commonly searched types of Pharmacovigilance jobs in Reston, VA?

The most popular types of Pharmacovigilance jobs in Reston, VA are:

What are popular job titles related to Remote Pharmacovigilance jobs in Reston, VA?

For Remote Pharmacovigilance jobs in Reston, VA, the most frequently searched job titles are:

What job categories do people searching Remote Pharmacovigilance jobs in Reston, VA look for?

The top searched job categories for Remote Pharmacovigilance jobs in Reston, VA are:

What cities near Reston, VA are hiring for Remote Pharmacovigilance jobs?

Cities near Reston, VA with the most Remote Pharmacovigilance job openings:

Infographic showing various Remote Pharmacovigilance job openings in Reston, VA as of August 2026, with employment types broken down into 77% Full Time, and 23% Contract. Highlights an 100% Remote job distribution, with an average salary of $100,025 per year, or $48.1 per hour.

Pharmacovigilance Expert - Remote

YO AI Labs

Washington, DC โ€ข Remote

$70 - $80/hr

Full-time

Posted 14 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.