2

Remote Pharmacovigilance Jobs (NOW HIRING)

Pharmacovigilance Expert

El Paso, TX 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

Peoria, AZ 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

Saint Louis, MO 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 ...

Pharmacovigilance Expert

Hollywood, FL 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

Spokane, WA 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

Plano, TX 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

Springfield, IL 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

Beaumont, TX 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 ...

Pharmacovigilance Expert

Kent, WA 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 ...

Pharmacovigilance Expert

Carrollton, TX 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 ...

Pharmacovigilance Expert

Lowell, MA 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 ...

Pharmacovigilance Expert

Charleston, SC 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

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

Centennial, CO 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

Orlando, FL 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 ...

Showing results 41-60

Remote Pharmacovigilance information

See salary details

$22

$46

$83

How much do remote pharmacovigilance jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for remote pharmacovigilance 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 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 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 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 cities are hiring for Remote Pharmacovigilance jobs? Cities with the most Remote 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 Remote Pharmacovigilance jobs? States with the most job openings for Remote Pharmacovigilance jobs include:
Infographic showing various Remote Pharmacovigilance job openings in the United States 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 $96,145 per year, or $46.2 per hour.

Pharmacovigilance Expert

micro1 AI

El Paso, TX โ€ข Remote

$70 - $80/hr

Part-time

Posted 4 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 โ€” 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.