Parexel Hiring 2026 | Patient Safety Associate I (Drug Safety) – Remote US Job

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Parexel Recruitment 2026 – Remote Pharmacovigilance Job

If you’re aiming to start or grow your career in pharmacovigilance and drug safety, this opportunity is worth exploring.
Parexel is hiring for the role of Patient Safety Associate I (Drug Safety Associate I) for a fully remote position in the United States.

This role is ideal for life sciences graduates and early-career professionals looking to gain real-world exposure in global safety operations.

About Parexel

Parexel is a globally recognized Clinical Research Organization (CRO) offering:

  • Clinical trial management
  • Regulatory consulting services
  • Drug safety and pharmacovigilance solutions

The company partners with pharmaceutical and biotech organizations worldwide to ensure safe, effective, and compliant drug development.

Job Details

  • Company Name: Parexel
  • Role: Patient Safety Associate I (Drug Safety Associate I)
  • Department: Pharmacovigilance / Medical Sciences
  • Experience: 0–3+ Years (Foundational knowledge required)
  • Qualification: Bachelor’s in Life Sciences or related field
  • Location: United States (Remote)
  • Work Type: Fully Remote

Eligibility Criteria

  • Bachelor’s degree in:
    • Life Sciences
    • Pharmacy
    • Microbiology
    • Biochemistry
    • Biotechnology
  • Basic understanding of drug safety and pharmacovigilance processes

Required Skills

  • Knowledge of pharmacovigilance regulations and guidelines
  • Understanding of clinical trials and post-marketing safety
  • Proficiency in MS Office (Excel, Word, PowerPoint)
  • Strong attention to detail and analytical thinking
  • Good communication and documentation skills
  • Ability to manage tasks independently and within teams

Key Responsibilities

  • Process and review Individual Case Safety Reports (ICSRs)
  • Perform literature search and safety data screening
  • Support signal detection and risk evaluation activities
  • Prepare and submit safety reports to regulatory authorities
  • Maintain tracking systems and compliance documentation
  • Assist in aggregate reports and Trial Master File (TMF) activities

Salary & Benefits

  • Competitive salary and total rewards package
  • Flexible remote work environment
  • Learning and development opportunities
  • Exposure to global pharmacovigilance operations
  • Inclusive and collaborative workplace culture

How to Apply

Interested candidates can apply through the official Parexel career portal.

Job ID: R0000039458

Submit your application online and begin your journey in drug safety.

Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Parexel career page.

Parexel Hiring 2026

APPLY FOR THIS JOB

Interview Process

  • No walk-in interview
  • Standard online recruitment process

Why You Should Join Parexel

  • Work with a leading global CRO
  • Gain hands-on experience in drug safety and regulatory reporting
  • Exposure to multiple therapeutic areas
  • Strong career growth and learning support
  • Opportunity to work on impactful healthcare projects

FAQs

1. What experience is required for this role?

Candidates with 0–3+ years and basic pharmacovigilance knowledge can apply. Prior experience in drug safety is an advantage.

2. What qualifications are required?

A Bachelor’s degree in Life Sciences or related fields is required.

3. Is this a remote job?

Yes, this is a fully remote role within the United States.

4. What areas will I work in?

You will gain exposure to ICSR processing, literature review, and safety reporting across multiple therapeutic areas.

5. How do I apply?

Apply online via the Parexel career portal using Job ID R0000039458.

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