Parexel Hiring Patient Safety Associates | Pharmacy Freshers Eligible
Looking for a Pharma Freshers Job in the clinical research and drug safety industry? Parexel is hiring for the position of Patient Safety Associate I in India. This Pharmacovigilance Job is an excellent opportunity for 2025 and 2026 graduates from Pharmacy, PharmD, and related fields to begin a rewarding career in drug safety, regulatory compliance, and clinical research.
- Position: Patient Safety Associate
- Location: India-Mohali, India – Hyderabad
- Job Requisition ID: R0000042958
About the Company
Parexel is a global clinical research organization committed to improving the world’s health. From clinical trials to regulatory, consulting, and market access services, Parexel supports the development of therapies that benefit patients worldwide. The organization focuses on innovation, empathy, quality, and regulatory excellence across all areas of clinical development.
Job Description
Parexel is looking for a Patient Safety Associate to support pharmacovigilance and drug safety activities. The role involves reviewing and processing safety data, ensuring compliance with regulatory requirements, and helping prepare accurate safety reports for clinical trials and marketed products while following global guidelines and SOPs.
Key Responsibilities
- Process Individual Case Safety Reports (ICSRs) from various sources, including data entry, coding (Medical Dictionary for Regulatory Activities [MedDRA]), narrative writing, and quality checks.
- Perform literature searches and reviews to identify potential adverse drug reactions and safety signals.
- Support safety submissions to regulatory authorities, ethics committees, and other stakeholders within required timelines.
- Assist in signal detection, compliance tracking, and the generation of safety metrics.
- Ensure accuracy, completeness, and regulatory compliance of safety data and documentation.
- Coordinate follow-ups, query management, and reconciliation activities with internal teams and affiliates.
- Support the preparation of aggregate reports and maintain safety reporting schedules.
- Contribute to regulatory intelligence activities by tracking safety reporting requirements and updates.
- Participate in audits, inspections, and quality improvement initiatives as required.
- Collaborate with cross-functional teams and support client communication under supervision.
Qualifications & Skills
- Master’s Degree in Pharmacy, or related field, or PharmD degrees.
- Eligible candidates: 2025 and 2026 graduates only.
- Basic knowledge of pharmacovigilance, ICH guidelines, and global safety reporting requirements.
- Strong attention to detail and analytical skills.
- Good communication, organization, and time management abilities.
- Proficiency in MS Office and familiarity with safety databases is advantageous.
- Ability to work effectively in a team and manage multiple tasks in a deadline-driven environment.
Preferred Experience
- Prior experience or internship in pharmacovigilance, clinical research, or a healthcare setting is preferred.
