ZipRecruiter

Log In

2

Remote Drug Safety Associate Jobs in Rhode Island

micro1 AI

Pharmacovigilance Expert

Providence, RI · 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

Providence, RI · 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 ...

Morley

Vehicle Return Clerk (Remote - Michigan)

Carolina, RI · Remote

$17 - $22.75/hr

Must have the ability to pass a pre-employment background check and drug screen * High school ... Associate wellness program with rewards for annual checkups * Programs to quit tobacco use and ...

Morley

Vehicle Return Clerk (Remote - Michigan)

Carolina, RI · Remote

$17 - $22.75/hr

Must have the ability to pass a pre-employment background check and drug screen * High school ... Associate wellness program with rewards for annual checkups * Programs to quit tobacco use and ...

Morley

Meeting and Event Coordinator (Remote)

Carolina, RI · Remote

$20.50 - $27.25/hr

Act as a liaison between sales associates, vendors and clients * Manage client expectations through ... Must have the ability to pass a pre-employment background check and drug screen * Bachelor's degree ...

New

GXO Logistics

Safety Supervisor - 1st Shift

NC · On-site +1

As the Supervisor, Environmental Health and Safety (EHS) you'll oversee the EHS team to ensure ... pre-employment drug test. The above statements are intended to describe the general nature and ...

Harris

(Remote) Software Engineer

Carolina, RI · Remote

Associates degree in Computer Science, Engineering, or a related field. * Proven experience as a ... safety, and healthcare software verticals. Our success has been realized through investments in our ...

Harris

Associate, Corporate Development

Carolina, RI · On-site +1

$70K - $90K/yr

Preference for Toronto, but open to remote candidates (within North America) Reports to: Director ... public safety market. * Maintain regular communication to keep prospects engaged and ensure ...

next page

Showing results 1-20

All JobsDrug Safety Associate JobsRemote Drug Safety Associate JobsRemote Drug Safety Associate Jobs in Rhode Island

Remote Drug Safety Associate information

See Rhode Island salary details

$12

$48

$84

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

As of Aug 9, 2026, the average hourly pay for remote drug safety associate in Rhode Island is $48.13, according to ZipRecruiter salary data. Most workers in this role earn between $37.64 and $54.38 per hour, depending on experience, location, and employer.

What does a remote drug safety associate do?

A typical workday for a Remote Drug Safety Associate involves reviewing and processing adverse event reports, entering data into safety databases, and preparing regulatory submissions. You may also participate in teleconferences with cross-functional global teams, respond to queries from regulatory bodies, and support ongoing safety surveillance activities. The role generally requires self-motivation and strong organizational skills to manage tasks independently while collaborating virtually with colleagues in pharmacovigilance, clinical, and regulatory departments. Flexible work schedules and regular online meetings are common, making time management essential in a remote setting.

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

To thrive as a Remote Drug Safety Associate, you need a background in life sciences, pharmacovigilance, and regulatory compliance, often supported by a relevant degree (such as pharmacy, nursing, or a related field). Familiarity with safety databases like Argus or ARISg, as well as certifications such as Drug Safety Certified Professional (DSCP), is common in this role. Strong attention to detail, clear written communication, and the ability to work independently are key soft skills. These competencies help ensure drug safety information is managed accurately and efficiently in a remote environment, contributing to patient safety and regulatory compliance.

What is a remote drug safety associate?

A Remote Drug Safety Associate is responsible for monitoring, assessing, and reporting adverse drug reactions (ADRs) to ensure medication safety and regulatory compliance. They review patient safety data, prepare safety reports, and liaise with healthcare professionals and regulatory agencies. Working remotely, they use specialized databases and communication tools to track and analyze drug safety information. Their role is crucial in ensuring that pharmaceuticals remain safe for consumers while complying with industry regulations.

What are popular job titles related to Remote Drug Safety Associate jobs in Rhode Island? For Remote Drug Safety Associate jobs in Rhode Island, the most frequently searched job titles are:
What job categories do people searching Remote Drug Safety Associate jobs in Rhode Island look for? The top searched job categories for Remote Drug Safety Associate jobs in Rhode Island are:
What cities in Rhode Island are hiring for Remote Drug Safety Associate jobs? Cities in Rhode Island with the most Remote Drug Safety Associate job openings:
Remote Drug Safety Associate jobs near you
Infographic showing various Remote Drug Safety Associate job openings in Rhode Island as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $100,102 per year, or $48.1 per hour.

Pharmacovigilance Expert

micro1 AI

Providence, RI • Remote

$70 - $80/hr

Part-time

Posted 5 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.

Apply