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

Parexel, a global clinical research organization, is hiring for the role of Patient Safety Associate I at its Mohali and Hyderabad locations. This opportunity is ideal for B.Pharm and M.Pharm graduates with 0–2 years of experience who are looking to start or build their career in pharmacovigilance and drug safety operations.

The role focuses on supporting safety case processing, adverse event management, safety data review, and compliance with global pharmacovigilance regulations. Candidates will work within a structured, regulated environment, collaborating with global teams to ensure high‑quality patient safety outcomes.

This is a strong entry‑level opportunity for professionals aiming to grow within the global pharmacovigilance industry and develop long‑term careers in clinical safety operations.

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Job Overview

• Position: Patient Safety Associate I
• Department:PV
• Location: Hyderabad, Mohali India
• Experience: 0 to 2 Years
• Qualification: B.Pharm, M.Pharm
• Job Type: Full-Time

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Key Responsibilities – Patient Safety Associate I

• Monitor incoming safety reports from multiple sources including mailboxes, EudraVigilance (EV), and biomedical literature searches.
• Perform literature searches as per defined search strategies and identify valid cases for entry into the safety database.
• Triage incoming reports to assess completeness, legibility, and case validity, including review of abstracts, articles, and citations.
• Create safety cases in the pharmacovigilance database, perform accurate data entry, and advance cases through defined workflow steps.
• Compare and analyze affiliate‑reported data against information available in the client system to ensure consistency.
• Review cases for medical cohesiveness and consistency.
• Perform product coding, ensure accurate MedDRA coding in accordance with MedDRA Term Selection: Points to Consider.
• Assess seriousness, causality, and expectedness of reported events.
• Prepare medically sound case narratives based on reported safety information.
• Initiate and manage case follow‑up queries as required.
• Perform quality and validation checks to ensure case accuracy and regulatory compliance.
• Support ICSR compliance activities, including late case investigations, root‑cause analysis for delays, and collection of supporting documentation.
• Prepare required ADR forms or coversheets.
• Support expedited reporting procedures, quality review of line listings and tabulations, and adherence to local safety reporting requirements.
• Register products and organizations with regulatory authorities for electronic reporting on behalf of sponsors.
• Maintain product records including new product additions, removal of withdrawn products, expired licenses, or MAH transfer updates in client systems.
• Generate, report, and reconcile compliance metrics in collaboration with internal teams, clients, and external partners.
• Support additional PV activities such as End of Study Unblinding (EOSU), case corrections, case deletion/deactivation requests, recoding activities, MAH reporting, safety notifications, Patient Oriented Programs (POP), and Social Media safety activities, as applicable.
• Complete assigned tasks within timelines and report challenges or risks promptly to supervisors.

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Required Skills & Qualifications

• Education: B.Pharm, M.Pharm, or Pharm.D only.
• Experience: 0–2 years of experience in pharmacovigilance, drug safety, or safety data management.
• Core Skills
  • Strong attention to detail to ensure accuracy in safety data processing.
  • Solid analytical skills for case assessment and problem resolution.
  • Good written and verbal communication skills.
  • Ability to collaborate effectively within cross‑functional teams.
  • Willingness to learn continuously and adapt to evolving PV processes.
• Pharmacovigilance Knowledge: Completion of a pharmacovigilance course or certification, or good knowledge of medical terminology and global drug safety regulations.
• Scientific Exposure: Publications in peer‑reviewed scientific journals.
• Digital & AI Skills
  • Experience using AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and improve productivity.
  • Curiosity to explore responsible and ethical use of AI, including risk management and compliance considerations.

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Why Join Paraxel?

• Global CRO Leadership
• Join a leading global Contract Research Organization with a strong presence across regulated markets, supporting pharmaceutical and biotech companies worldwide.
• Strong Foundation in Pharmacovigilance
• Gain hands‑on exposure to ICSR processing, safety data management, literature monitoring, regulatory reporting, and compliance with global pharmacovigilance standards.
• Entry‑Level Growth Opportunity
• The Patient Safety Associate I role is designed for freshers and early‑career professionals, providing structured onboarding and continuous learning in drug safety operations.

How to Apply

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

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