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Remote Drug Safety Associate Jobs in California (NOW HIRING)

Abbott

Technician I, Remote Care

Pleasanton, CA · On-site +1

$25 - $31/hr

Troubleshooting skills. Med background not necessary but preferred. * 1-2 years exp or Associates ... Medical and Prescription Drug Plans * Dental Plan * Vision Plan * Health Savings Account (for High ...

Harbor Freight Tools

Merchant - Remote

Calabasas, CA · On-site +1

$117K - $176K/yr

Associates will accrue paid time off up to 236 hours per year (inclusive of PTO, floating holidays ... Safety Must be able to perform this job safely in accordance with standard operating procedures and ...

ICON

Senior Clinical Research Associate

Los Angeles, CA · On-site +1

$110K - $138K/yr

Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site ... subject safety in the client's trials * May perform oversight activities to assess monitoring ...

Corvel

Content Marketing Associate

Irvine, CA · Remote

$83K - $139K/yr

The Content Marketing Associate will lead content initiatives, manage CorVel's LinkedIn account ... drug free workplace, and complies with ADA regulations as applicable. #LI-Remote

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Remote Drug Safety Associate information

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$12

$48

$84

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

As of Sep 5, 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 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 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 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 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $100,878 per year, or $48.5 per hour.

Biology Research Scientist - Remote

YO AI Labs

Los Angeles, CA • Remote

$50 - $70/hr

Full-time

Posted 10 days ago

Job description

Biology Research Scientist

Job Type: Contractor
Location: Remote
Hours: 10–20 hours/week
Duration: 1–2 months minimum, with likely extension
Start: Immediate

Job Overview

We are seeking experienced Biology Research Scientists to support a project focused on validating protein target assignments against primary scientific sources and UniProt records.

You will review research papers and patents, identify target assignment errors, propose corrected UniProt accessions, and provide concise, evidence-based scientific reasoning.

Key Responsibilities
  • Review primary research papers and patents to verify protein target assignments.
  • Compare target assignments against UniProt and identify discrepancies.
  • Classify target assignment errors using a structured taxonomy.
  • Propose accurate UniProt accessions where assignments are incorrect.
  • Document clear, concise, evidence-grounded reasoning for each determination.
  • Apply expertise in pharmacology, biochemistry, molecular biology, or chemical biology to evaluate target relationships.
Required Skills
  • Protein Target Identification
  • UniProt
  • Primary Literature Review
  • Protein Biochemistry
  • Molecular Biology
  • Pharmacology
  • Binding & Functional Assays
  • Scientific Data Interpretation
  • Evidence-Based Reasoning
  • Technical Documentation
Qualifications
  • BA/BS + 5 years, MS + 2 years, or PhD with relevant industry/drug discovery experience.
  • Background in pharmacology, biochemistry, molecular biology, or chemical biology within biotech, pharma, or CRO environments.
  • Hands-on experience with assays such as SPR, TR-FRET, radioligand binding, kinase assays, or GPCR functional assays.
  • Experience interpreting IC50, Ki, and Kd data.
  • Currently active in a bench-based research, scientist, or associate scientist role.
  • Working knowledge of UniProt or related workflows such as SAR, HTS, target validation, biochemical profiling, or IND-enabling studies.
Nice to Have
  • Experience with ChEMBL, BindingDB, or PubChem.
  • Selectivity profiling or counterscreening experience.
  • Understanding of agonist/antagonist vs. activator/inhibitor distinctions.
Screening Questions
  1. What is your highest relevant degree and how many years of industry research experience do you have?
  2. What is your experience with protein target identification and UniProt?
  3. Which binding or functional assays have you performed hands-on?
  4. Do you have experience interpreting IC50, Ki, or Kd data?
  5. Have you worked with ChEMBL, BindingDB, or PubChem?
  6. Are you currently bench-active in a research or scientist role?
  7. Are you available for 10–20 hours per week with an immediate start?