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Remote Drug Safety Intern Jobs in Raleigh, NC (NOW HIRING)

micro1 AI

Pharmacovigilance Expert

Durham, NC · 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 ...

micro1 AI

Pharmacovigilance Expert

Cary, NC · 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 ...

micro1 AI

Pharmacovigilance Expert

Raleigh, NC · 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 ...

micro1 AI

Clinical Pharmacy Technicians

Durham, NC · 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 ...

micro1 AI

Clinical Pharmacy Technicians

Raleigh, NC · 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 ...

micro1 AI

Clinical Pharmacy Technicians

Cary, NC · 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 ...

Raymond

Senior Structural Engineer

Raleigh, NC · On-site +1

$97K - $132K/yr

Savannah, GA / Remote (Hybrid options available) About Raymond: We are a progressive, forward ... quality, safety, and performance. Key Responsibilities: * Serve as engineer-of-record and ...

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Remote Drug Safety Intern information

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How much do remote drug safety intern jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for remote drug safety intern in Raleigh, NC is $16.56, according to ZipRecruiter salary data. Most workers in this role earn between $14.04 and $18.70 per hour, depending on experience, location, and employer.

What does a remote drug safety intern do?

As a Remote Drug Safety Intern, you will typically assist with processing and reviewing adverse event reports, maintaining safety databases, and supporting the preparation of regulatory documents. You may also be involved in literature surveillance and help ensure compliance with global pharmacovigilance standards. Collaboration with cross-functional teams, such as clinical operations and regulatory affairs, is common, allowing you to gain exposure to various aspects of drug safety. These experiences provide valuable insight into the industry and can help build a strong foundation for a future career in pharmacovigilance or regulatory roles.

What are the key skills and qualifications needed to thrive as a remote drug safety intern?

To thrive as a Remote Drug Safety Intern, you need a background in life sciences or pharmacy, attention to detail, and a strong understanding of pharmacovigilance principles. Familiarity with safety databases, MedDRA coding, and regulatory reporting systems such as Argus or ARISg is typically required. Excellent communication, organizational skills, and the ability to work independently are highly valued soft skills. These competencies ensure accurate adverse event reporting, regulatory compliance, and effective collaboration in a remote environment.

What is a remote drug safety intern?

Remote Drug Safety Interns are students or recent graduates who work virtually with pharmaceutical or biotechnology companies to support drug safety and pharmacovigilance activities. Their responsibilities typically include assisting with the collection, documentation, and analysis of adverse event reports, ensuring compliance with regulatory guidelines, and supporting safety data review processes. Working remotely, these interns collaborate with safety teams using digital tools, gaining hands-on experience in monitoring the safety of medicinal products while developing industry-specific skills. This role is ideal for those interested in regulatory affairs, clinical research, or public health, and offers exposure to the critical processes that ensure medication safety for patients.
What are the most commonly searched types of Remote Drug Safety jobs in Raleigh, NC? The most popular types of Remote Drug Safety jobs in Raleigh, NC are:
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Remote Drug Safety Intern jobs near you
Infographic showing various Remote Drug Safety Intern job openings in Raleigh, NC as of June 2026, with employment types broken down into 6% Internship, 68% Full Time, 20% Part Time, and 6% Contract. Highlights an 100% Remote job distribution, with an average salary of $34,446 per year, or $16.6 per hour.

Pharmacovigilance Expert

micro1 AI

Durham, NC • Remote

$70 - $80/hr

Part-time

Posted 7 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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