ZipRecruiter

Log In

2

Remote Drug Safety Associate Jobs in California (NOW HIRING)

YO AI Labs

Pharmacovigilance Expert - Remote

San Jose, CA · Remote

$70 - $80/hr

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 ...

New

Mercor

AI Safety Expert - Red Team

San Francisco, CA · Remote

$48 - $62/hr

Remote Role Responsibilities * Red team conversational AI models and agents to identify jailbreaks, prompt injections, misuse cases, and bias exploitation. * Generate high-quality human data by ...

Mercor

AI Safety Expert - Red Teaming

San Francisco, CA · Remote

$48 - $62/hr

Remote Role Responsibilities * Red team conversational AI models and agents to identify jailbreaks, prompt injections, misuse cases, and bias exploitation. * Generate high-quality human data by ...

MiniMed

Medical Safety Spec

Northridge, CA · On-site +1

About the Role The Medical Safety (MS) Specialist is responsible for providing medical expertise and assessment to support patient safety throughout the lifecycle as both an advocate for patient ...

next page

Showing results 1-20

All JobsDrug Safety Associate JobsRemote Drug Safety Associate JobsRemote Drug Safety Associate Jobs in California

Remote Drug Safety Associate information

See California salary details

$12

$48

$84

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

As of Aug 12, 2026, the average hourly pay for remote drug safety associate in California is $48.50, according to ZipRecruiter salary data. Most workers in this role earn between $37.98 and $54.81 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 the most commonly searched types of Remote Drug Safety jobs in California? The most popular types of Remote Drug Safety jobs in California are:
What are popular job titles related to Remote Drug Safety Associate jobs in California? For Remote Drug Safety Associate jobs in California, the most frequently searched job titles are:
What job categories do people searching Remote Drug Safety Associate jobs in California look for? The top searched job categories for Remote Drug Safety Associate jobs in California are:
What cities in California are hiring for Remote Drug Safety Associate jobs? Cities in California 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 California as of August 2026, with employment types broken down into 81% Full Time, 15% Part Time, and 4% Temporary. Highlights an 100% Remote job distribution, with an average salary of $100,878 per year, or $48.5 per hour.

Pharmacovigilance Expert - Remote

YO AI Labs

Palo Alto, CA • Remote

Full-time

Posted yesterday

New

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.