Paraxel Hiring for Patient Safety Associate I Role: PV Jobs 2026

ByPharma Hiring Hub

Parexel, a leading global CRO, is hiring Patient Safety Associate I roles across India. This entry‑level opportunity is ideal for Life Sciences and Pharmacy graduates who want to begin a career in pharmacovigilance and drug safety.
In this role, you’ll gain hands‑on experience in ICSR processing, MedDRA coding, global safety databases, compliance metrics, and regulatory safety submissions while working in a structured, training‑focused environment.

Patient safety associate at paraxel

Job Overview

  • Position: Patient Safety Associate I
  • Department: PV
  • Location: Bengaluru, Hyderabad, Mohali
  • Experience: 2 to 6 Years
  • Qualification: Degree in Life Sciences, Health Sciences, or Biomedical Sciences, such as Pharmacy, Microbiology, Biochemistry, Biotechnology, or a related discipline
  • Job Type: Full-Time

Key Responsibilities – Patient Safety Associate I

  • Learn safety profiles, regulations, project workflows, and maintain proper documentation.
  • Support audits, compliance tasks, and complete training & timesheets on time.
  • Process ICSRs: monitor incoming reports, triage, perform data entry, MedDRA coding, follow‑ups, query management, and write narratives.
  • Perform QC checks, support late case investigations, compliance metrics, and handle additional case‑processing tasks as assigned.
  • Submit ICSRs and periodic reports to Health Authorities; maintain reporting schedules; support global safety submissions and eTMF documentation.
  • Conduct literature searches, screen articles for ADR signals, perform QC, and coordinate with medical reviewers.
  • Assist affiliates with safety communication, product updates, literature screening, translation needs, and reconciliation tasks.
  • Support regulatory submissions, lifecycle changes, data validation, xEVMPD, and generating quality reports.
  • Maintain regulatory intelligence for assigned countries; update trackers/databases and support GPIO activities.

Required Skills & Qualification:

Skills

  • Basic understanding of drug safety regulations and pharmacovigilance processes.
  • Entry‑level analytical and problem‑solving abilities.
  • Good communication skills for clear documentation and teamwork.
  • Strong organizational and time‑management capabilities.
  • Introductory familiarity with PV systems and safety databases.
  • Basic computer skills, including proficiency in Windows and MS Office applications.

Knowledge & Experience

  • Prior experience in a healthcare environment is an added advantage.
  • Basic knowledge of healthcare and medical terminology.
  • Ability to learn and understand ICH guidelines and regional PV requirements.
  • Strong desire to learn and grow in pharmacovigilance and drug safety.
  • Genuine interest in the pharmaceutical or healthcare domain.

Education

Equivalent qualifications or relevant work experience may also be considered. Degree in Life Sciences, Health Sciences, or Biomedical Sciences
(e.g., Pharmacy, Microbiology, Biochemistry, Biotechnology, etc.)

Why Join Paraxel?

Global CRO Exposure:
Work with a world‑leading CRO and gain hands‑on experience with international drug safety processes.

Structured Training:
Access to comprehensive LMS‑based training, helping you quickly build PV and compliance skills.

Audit & Inspection Readiness:
Learn how global audits and regulatory inspections work—an essential skill for long‑term PV careers.

Regulatory Submission Learning:
Get exposure to ICSR submissions, periodic reports, and global safety reporting requirements.

Career Growth Path:
Strong potential to grow into Senior Drug Safety Associate, Safety Specialist, or Case Quality Reviewer roles.

Work on Global Projects:
Contribute to international clinical development and drug safety projects, collaborating with global teams.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.

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FAQ – Patient Safety Associate I

1. What skills are important for this role?

Basic PV knowledge, analytical ability, good communication, time management, familiarity with PV systems/databases, and proficiency in Windows + MS Office.

2. Will I be trained?

Yes. Parexel offers structured training, hands‑on project exposure, and ongoing skill development modules through their Learning Management System (LMS).

3. What kind of work environment can I expect?

You’ll work within global safety teams, follow SOPs, assist senior associates, and gain exposure to audits, inspections, and global submissions.

4. What tools or systems will I work with?

PV databases, MedDRA coding tools, global safety reporting platforms, and standard clinical documentation systems.

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