Parexel Hiring Patient Safety Associate I in Mohali, India

Parexel is hiring a Patient Safety Associate I in Mohali, India, for pharmacovigilance and drug safety operations. This Parexel Mohali pharmacovigilance opening is an on-site role. Eligible candidates are 2025 and 2026 graduates. The end date to apply is November 9, 2026.

Job Details

Company: Parexel

Job Title: Patient Safety Associate I

Location: India-Mohali

Work Mode: On-site

Posted: Posted Today

End Date: November 9, 2026 (3 days left to apply)

Job Requisition ID: R0000047639

Parexel Mohali Pharmacovigilance Job Description

We are seeking a detail-oriented Patient Safety Associate I to join our team in on-site capacity, based in Mohali. As a Patient Safety Associate, you will support pharmacovigilance and drug safety operations across clinical trials and post-marketing activities. This position plays a key role in processing safety data, ensuring regulatory compliance, and contributing to high-quality safety reporting in line with global regulations and standard operating procedures (SOPs). You’ll collaborate with cross-functional teams, follow industry-standard processes, and help ensure that patient safety data is accurate, complete, and ready for regulators.

Responsibilities include processing Individual Case Safety Reports (ICSRs), supporting safety submissions to regulatory authorities, and maintaining the accuracy and completeness of safety data, with opportunities to deepen your expertise and strengthen the quality of safety reporting.

You’ll join a fast-paced, growth-oriented environment focused on making a meaningful impact through safety data processing, signal detection, and regulatory reporting. With diverse teams and continuous learning opportunities, the Patient Safety Associate can explore career paths and expand skills across pharmacovigilance and clinical research.

Key Responsibilities

  • Process Individual Case Safety Reports (ICSRs) from various sources, including data entry, medical coding using the 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 the 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.

Parexel Mohali Pharmacovigilance Eligibility Criteria

  • Master’s in Pharmacy, or a PharmD or BDS degree or Master’s in a related field in Life Sciences.
  • Eligible candidates are 2025 and 2026 graduates only.
  • Basic knowledge of pharmacovigilance, International Council for Harmonisation (ICH) guidelines, and global safety reporting requirements.
  • Strong attention to detail and analytical skills.
  • Good communication, organization, and time management abilities.
  • Ability to work effectively in a team and manage multiple tasks in a deadline-driven environment.

Required Skills

You’ll thrive in this Parexel Mohali pharmacovigilance role if you bring:

  • Strengths in attention to detail, analytical thinking, and time management.
  • A background in life sciences, pharmacy, or a related field.
  • The ability to collaborate across teams and communicate clearly.
  • A patient-focused mindset and a commitment to high-quality work.
  • Comfort working with Microsoft Office and a willingness to learn safety databases and processes.

Additional Information

Preferred Qualifications:

  • Proficiency in Microsoft Office.
  • Familiarity with safety databases.

About Parexel: Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.

We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.

CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE

CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE

Apply online for the Parexel Mohali pharmacovigilance job through the link above before November 9, 2026.