Freshers Life Science Jobs at Parexel | Clinical Research Role
Are you looking for Freshers Life Science Jobs in the clinical research industry? Parexel Careers has announced an excellent opportunity for the role of Patient Safety Associate I in Mohali, India. This Clinical Research Job is ideal for 2025 and 2026 graduates with a Master’s degree in Life Sciences, Pharmacy, PharmD, or BDS who are interested in pharmacovigilance, drug safety, and global clinical research. Explore the complete eligibility criteria, responsibilities, qualifications, and application details below.
About Parexel
Parexel is a leading global clinical research organisation (CRO) dedicated to improving the world’s health by supporting the development of innovative therapies. The company provides end-to-end clinical development solutions, including clinical trials, regulatory consulting, pharmacovigilance, market access, and medical communications. With a strong presence across the globe, Parexel focuses on delivering high-quality research while maintaining patient safety, regulatory compliance, and scientific excellence. Working at Parexel offers professionals valuable exposure to global clinical research, making it one of the most preferred employers for Life Science graduates seeking careers in pharmacovigilance and clinical research.
- Job Location: Mohali, India
- Job Type: Full-Time
- Application Deadline: July 2, 2026
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 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
- Master’s Degree in Life Sciences, Pharmacy, or related field, or PharmD or BDS degrees.
- Eligible candidates: 2025 and 2026 graduates only.
Experience
Prior experience or internship in pharmacovigilance, clinical research, or a healthcare setting is preferred.
Skills Needed
- Basic knowledge of pharmacovigilance, ICH guidelines, and global safety reporting requirements.
- Strong attention to detail and analytical skills.
- Good communication, organisation, 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.
If you are searching for Freshers Life Science Jobs, this opportunity through Parexel Careers is an excellent way to begin your career in pharmacovigilance and drug safety. These Clinical Research Jobs offer exposure to global safety reporting, regulatory compliance, and clinical development processes, making them an ideal career choice for Life Science and Pharmacy graduates.
