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Patient Safety Associate I (Drug Safety Associate I) at Parexel – Remote US Opportunity

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Parexel is hiring a Patient Safety Associate I (Drug Safety Associate I) for a remote role in the United States. This is an excellent pharma jobs opportunity for life sciences graduates and early-career professionals to build a career in pharmacovigilance and patient safety.

About the Company

Parexel is a leading global clinical research organization (CRO) providing integrated biopharmaceutical services to help clients accelerate drug development and commercialization. Known for scientific excellence, innovation, and regulatory compliance, Parexel partners with pharmaceutical and biotech companies worldwide.

The company is committed to diversity, inclusion, and employee development, offering a collaborative environment where professionals can make a meaningful impact on patient health through high-quality clinical and safety services.

Job Details

  • Company Name: Parexel
  • Experience: Foundational knowledge preferred; 2+ years in post-marketing and 3+ years in Drug Safety ideal
  • Qualification: Bachelor’s degree in Life Sciences, Health Sciences, Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology) or equivalent
  • Location: United States (Remote)
  • Work Type: Remote

Job Description

Parexel is seeking a Patient Safety Associate I to support drug safety and pharmacovigilance activities. The role involves processing Individual Case Safety Reports (ICSRs), literature reviews, signal detection support, and regulatory submissions. This position offers foundational exposure to clinical trials and post-marketing surveillance in a global CRO environment, ideal for building a career in patient safety.

Patient Safety Associate I (Drug Safety Associate I)

  • Department: Medical Sciences / Pharmacovigilance
  • Role: Patient Safety Associate I
  • Experience: 0–3+ Years (Foundational knowledge required)
  • Education/Qualification: Bachelor’s in Life Sciences or equivalent

Skills/Qualifications

  • Foundational knowledge of pharmacovigilance principles and drug safety regulations
  • Understanding of clinical trial and post-marketing safety requirements
  • Proficiency in MS Office (Word, Excel, PowerPoint) and ability to learn safety databases
  • Strong attention to detail, organizational, and time management skills
  • Excellent written and verbal communication skills
  • Ability to work independently and collaboratively in a team environment

Key Responsibilities

  • Review, triage, and process Individual Case Safety Reports (ICSRs)
  • Conduct literature searches and screen articles for safety signals
  • Support signal detection and management activities
  • Prepare and submit safety reports to regulatory authorities
  • Maintain regulatory intelligence and submission tracking
  • Assist in aggregate report preparation and TMF documentation

Benefits/Perks

  • Career growth in a global CRO leader
  • Structured learning and development programs
  • Exposure to diverse therapeutic areas and safety operations
  • Collaborative and inclusive work culture
  • Flexible remote work arrangement
  • Competitive total rewards package

How to Apply

Verified Post

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

Parexel is hiring a Patient Safety Associate I (Drug Safety Associate I) for a remote role in the United States.

🔗 Click below to apply directly for this job

Interested candidates can apply directly through the Parexel career portal using Job ID R0000039458.

For more pharma jobs and opportunities across India and globally, visit Pharma Recruiter.

Apply now and start your pharmacovigilance journey with Parexel!

Walk-in Interview Details

Not applicable (Standard online application process)

Why You Should Join

Parexel offers a dynamic, purpose-driven culture where innovation and patient safety are paramount. The company provides long-term career stability, recognition for contributions, and continuous learning opportunities in a global, collaborative environment. Joining Parexel means working on impactful projects that improve patient outcomes while building expertise in pharmacovigilance and clinical research.

FAQs

Q1: What experience is required for the Patient Safety Associate I role?

A: Foundational knowledge in drug safety; 2+ years post-marketing experience is ideal.

Q2: What qualifications are needed?

A: Bachelor’s degree in Life Sciences, Pharmacy, or related fields.

Q3: Is the position remote?

A: Yes, this is a fully remote role in the United States.

Q4: What therapeutic areas are involved?

A: Exposure to multiple areas including cardiology, neurology, oncology, and rare diseases.

Q5: How can I apply?

A: Submit your application online via the Parexel career portal with Job ID R0000039458.

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