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Remote Drug Safety Associate Jobs (NOW HIRING)

Company Description Medical Safety Physician 6-month assignment 100% Remote What are the three most ... adverse drug reactions, review medical inputs for into signal management and benefit-risk ...

Remote / Flexible Type: Part-Time Consultant (Expected 15-20 hrs/week) Therapeutic Area: Pediatric ... and drug safety, with a proven track record of leading safety functions and contributing to ...

Remote / Flexible Type: Part-Time Consultant (Expected 15-20 hrs/week) Therapeutic Area: Pediatric ... and drug safety, with a proven track record of leading safety functions and contributing to ...

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Remote Drug Safety Associate information

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$12

$49

$85

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

As of Jun 6, 2026, the average hourly pay for remote drug safety associate in the United States is $49.14, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $55.53 per hour, depending on experience, location, and employer.

What does a typical workday look like for a Remote Drug Safety Associate?

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 in the Remote Drug Safety Associate position, and why are they important?

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 job?

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.

More about Remote Drug Safety Associate jobs
What cities are hiring for Remote Drug Safety Associate jobs? Cities with the most Remote Drug Safety Associate job openings:
What are the most commonly searched types of Remote Drug Safety jobs? The most popular types of Remote Drug Safety jobs are:
What states have the most Remote Drug Safety Associate jobs? States with the most job openings for Remote Drug Safety Associate jobs include:
Infographic showing various Remote Drug Safety Associate job openings in the United States as of May 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

Pharmacovigilance Pharmacist

Pharmacy Careers

Fayetteville, NC • On-site, Remote

$53.50 - $64.25/hr

Other

Posted 24 days ago


Job description

Pharmacovigilance Pharmacist
Bring your clinical lens to the world of drug safety and reporting.
Key Responsibilities:

  • Analyze adverse event reports and clinical trial safety data.
  • Prepare regulatory submissions (e.g., MedWatch, PSURs).
  • Collaborate with medical affairs and clinical teams to address safety signals.

Qualifications:

  • PharmD with strong understanding of pharmacology.
  • Prior experience in drug safety or clinical data review is a plus.
  • Detail-oriented with excellent written communication.

Why Join Us?

  • Remote or hybrid options
  • Pharma industry training provided
  • Clear career path into global drug safety