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TFS HealthScience

A leading global Contract Research Organization is seeking a Drug Safety Officer to manage drug safety issues in compliance with regulations. The role involves overseeing clinical trials and ensuring ...

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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.

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Remote Drug Safety Associate jobs near you
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.
R0000038960 Patient Safety Associate I (Drug Safety Associate I)

R0000038960 Patient Safety Associate I (Drug Safety Associate I)

Parexel

Remote

Full-time

Posted 8 days ago

Job description

When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Make a Meaningful Impact in Global Patient Safety
At Parexel, we're dedicated to improving patient health worldwide. As a Patient Safety Associate I, you'll play a vital role in supporting drug safety, clinical trials, and post-marketing surveillance activities in post-market surveillance, with some exposure to clinical trials, ensuring full compliance with regulatory requirements and Standard Operating Procedures (SOPs).
As a Patient Safety Associate I, you'll be responsible for several key activities including processing Individual Case Safety Reports (ICSRs) from multiple sources with accuracy and efficiency, conducting comprehensive literature searches and reviews to identify safety signals, and supporting signal detection and management activities. You'll track and monitor regulatory information updates, assist in preparing and executing regulatory submissions, and contribute to the development of aggregate reports and study-specific safety documents. Where applicable, you'll also manage Medical and Product Dictionary activities. Your role will be crucial in maintaining compliance through quality reviews of safety deliverables, generating metrics and performance indicators for safety operations, investigating and documenting late deliverable incidents, and ensuring adherence to international and local regulatory reporting requirements.
We're looking for candidates with strong attention to detail and commitment to quality, an understanding of drug safety regulations and pharmacovigilance principles, excellent organizational and time management skills, the ability to work collaboratively in a team environment, and strong written and verbal communication skills. Join a global leader in Clinical Research Organization services, where you'll contribute to improving patient safety worldwide while developing your career in pharmacovigilance.
What You'll Do:
General Safety Operations
  • Follow project-specific procedures and regulatory standards.
  • Support basic compliance activities, documentation, metrics, and audit preparation.
  • Work collaboratively with team members and complete required training programs.

ICSR (Individual Case Safety Report) Processing
  • Review, triage, and process safety reports from various sources.
  • Perform data entry in safety databases with accuracy and medical consistency.
  • Assist with follow-ups, case narrative preparation, MedDRA coding, and quality checks.
  • Support compliance investigations and metrics reporting.
  • Prepares medically cohesive case narratives based upon the reported information.

Safety Submissions
  • Submit ICSRs and periodic safety reports to Health Authorities and stakeholders.
  • Maintain regulatory submission schedules and reporting rules.
  • Assist in audit preparation and regulatory intelligence updates.
  • Support global reporting configuration and compliance activities.

Literature Search & Review
  • Develop and maintain literature search strategies.
  • Screen published articles for potential safety signals or adverse events.
  • Conduct quality checks and manage journal reviews.
  • Collaborate with internal teams for full-text retrieval and assessment.

Affiliate Services
  • Support communication between global operations and local safety affiliates.
  • Assist with safety information exchange, translations, and compliance tasks.
  • Conduct literature monitoring and data reconciliation activities.

Regulatory Support
  • Maintain regulatory systems and product registrations.
  • Assist with submissions (eCTD), renewals, variations, and lifecycle management.
  • Verify data accuracy and generate quality and compliance reports.

Regulatory Intelligence
  • Research and maintain global safety reporting requirements.
  • Update regulatory intelligence databases and trackers.
  • Support day-to-day operations within the Global Pharmacovigilance Intelligence Office.

Your Knowledge & Experience:
  • Foundational knowledge of drug safety regulations and pharmacovigilance processes. Ideal candidate has 3+ years experience in Drug Safety.
  • 2+ years experience in a post marketing.
  • Experience in multiple therapeutic areas (cardiology, neurology, oncology, rare disease).
  • Strong attention to detail, organizational skills, and problem-solving ability.
  • Effective communication and willingness to work in a collaborative team environment.
  • Proficiency with MS Office and ability to learn safety systems/databases. Preference for those with Veeva Safety experience.

Education
  • Bachelor's degree in Life Sciences, Health Sciences, Biomedical Sciences
    (e.g., Pharmacy, Microbiology, Biochemistry, Biotechnology)
    or equivalent education/experience.

This role offers the flexibility to work from home in the US.
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EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
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About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983

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