Parexel Recruitment 2026
Looking to launch your career in pharmacovigilance and drug safety? Here’s an excellent opportunity for fresh graduates! Parexel, one of the world’s leading Clinical Research Organizations (CROs), is inviting applications for the Patient Safety Associate I position at its Mohali, Punjab office.
This role is specially designed for 2025 and 2026 graduates from pharmacy, life sciences, healthcare, and related disciplines who want to gain practical experience in Individual Case Safety Report (ICSR) processing, MedDRA coding, literature review, regulatory compliance, and global pharmacovigilance operations.
If you’re passionate about ensuring medicine safety and building a long-term career in clinical research, this could be the ideal first step.
Application Deadline: 11 August 2026 (as mentioned in the official job posting)
Parexel Recruitment 2026 – Job Overview
| Particular | Details |
|---|---|
| Company | Parexel |
| Job Role | Patient Safety Associate I |
| Department | Pharmacovigilance / Drug Safety |
| Job Location | Mohali, Punjab |
| Experience | Freshers / Entry-Level |
| Eligible Batch | 2025 & 2026 Graduates |
| Qualification | M.Pharm, Master’s in Life Sciences, PharmD, BDS or Related Field |
| Employment Type | Full-Time |
| Application Deadline | 11 August 2026 |
| Requisition ID | R0000044453 |
Important: Always verify eligibility criteria and vacancy status on Parexel’s official careers portal before applying.
About Parexel
Parexel is a globally recognized Clinical Research Organization (CRO) that partners with pharmaceutical, biotechnology, and medical device companies to accelerate the development of innovative healthcare solutions.
The company provides services across:
- Clinical Research
- Pharmacovigilance
- Regulatory Affairs
- Medical Writing
- Market Access
- Clinical Consulting
Working at Parexel offers fresh graduates exposure to international drug safety standards, regulatory requirements, and real-world clinical research projects.
Educational Qualification
Candidates meeting the following qualifications are eligible to apply:
- M.Pharm
- Master’s in Life Sciences
- Master’s in a Relevant Scientific Discipline
- PharmD
- BDS
Candidates from the 2025 and 2026 graduating batches are encouraged to apply.
Although previous work experience isn’t mandatory, basic knowledge of pharmacovigilance concepts will be an added advantage.
What Does a Patient Safety Associate Do?
A Patient Safety Associate helps monitor the safety of medicines after they are used by patients.
The role involves collecting, reviewing, documenting, and reporting adverse events while ensuring compliance with global pharmacovigilance regulations.
Freshers joining this role receive practical exposure to multiple drug safety activities, making it an excellent career foundation in pharmacovigilance.
Key Responsibilities
Selected candidates may work on:
✅ Individual Case Safety Report (ICSR) Processing
- Reviewing adverse event reports
- Data entry into safety databases
- Case validation
- Narrative writing
- Quality review
✅ MedDRA Coding
- Coding medical events using MedDRA terminology
- Maintaining coding accuracy
- Understanding medical terminology
✅ Literature Monitoring
- Reviewing published scientific literature
- Identifying safety-related information
- Supporting literature-based case processing
✅ Safety Reporting
- Assisting in regulatory safety submissions
- Supporting compliance with reporting timelines
- Documentation management
✅ Follow-Up Activities
- Requesting additional information
- Case reconciliation
- Query management
✅ Signal Detection Support
- Supporting safety trend identification
- Assisting senior pharmacovigilance professionals
✅ Aggregate Reporting
Exposure to:
- Periodic Safety Reports
- Benefit-Risk Documentation
- Reporting schedules
✅ Regulatory Compliance
- Following SOPs
- Maintaining data quality
- Supporting audit readiness
Skills Required
Freshers can strengthen their profile by having knowledge of:
Pharmacovigilance Basics
- Adverse Events (AE)
- Adverse Drug Reactions (ADR)
- Serious Adverse Events (SAE)
- ICSR Processing
- Safety Reporting
- Signal Detection
ICH Guidelines
Understanding basic international pharmacovigilance regulations is beneficial.
Medical Terminology
Knowledge of diseases, drugs, symptoms, and clinical terminology helps in accurate case processing.
MedDRA Awareness
Basic familiarity with MedDRA coding improves employability.
Computer Skills
Candidates should be comfortable using:
- Microsoft Word
- Excel
- Outlook
- PowerPoint
Knowledge of pharmacovigilance databases is an added advantage.
Communication Skills
The role requires clear written and verbal communication while working with global teams.
Why Freshers Should Apply
This position offers valuable exposure to the pharmaceutical industry’s drug safety function.
Some career benefits include:
- International CRO experience
- Practical pharmacovigilance training
- Global regulatory exposure
- Hands-on ICSR processing
- MedDRA coding experience
- Career growth in clinical research
Career Growth After Joining
Professionals can gradually progress into roles such as:
- Drug Safety Associate
- Pharmacovigilance Specialist
- Senior Patient Safety Associate
- Case Processing Specialist
- Aggregate Reporting Associate
- Signal Detection Analyst
- Safety Data Management Specialist
- Medical Reviewer
- Pharmacovigilance Quality Associate
- Safety Operations Manager
Career advancement depends on performance, project exposure, and continuous learning.
Resume Tips for Freshers
Before applying, ensure your resume highlights:
- Pharmacology knowledge
- Clinical Pharmacy
- Pharmacovigilance concepts
- Toxicology
- Clinical Research
- Medical Terminology
- Attention to detail
- Communication skills
- Academic projects
- Internships
- Certifications
- Workshops
A concise one-page ATS-friendly resume often performs better for entry-level positions.
How to Apply?
Eligible candidates should visit the official Parexel Careers portal and search for:
Patient Safety Associate I (Requisition ID: R0000044453)
Complete the online application form and upload your latest resume before the deadline.
Last Date to Apply: 11 August 2026
Apply Now 👇🏻
If the short link doesn’t open or has expired, use the official Parexel Careers portal instead:
Important Points Before Applying
✔ Check educational eligibility.
✔ Verify the application deadline.
✔ Update your resume.
✔ Ensure your contact details are correct.
✔ Understand basic pharmacovigilance concepts.
✔ Apply only through the official Parexel recruitment portal.
Final Thoughts
The Parexel Recruitment 2026 drive is a promising opportunity for fresh graduates looking to begin a career in pharmacovigilance, clinical research, and drug safety.
The Patient Safety Associate I role provides exposure to ICSR processing, MedDRA coding, literature monitoring, safety reporting, and regulatory compliance—skills that form the backbone of a successful pharmacovigilance career.
If you’re a 2025 or 2026 graduate with qualifications in M.Pharm, PharmD, Life Sciences, or BDS, don’t miss this opportunity. Prepare a strong resume, review the official job details carefully, and submit your application before the deadline.
Frequently Asked Questions (FAQs)
1. Who can apply for Parexel Recruitment 2026?
Candidates who completed M.Pharm, PharmD, BDS, or a Master’s in Life Sciences or related scientific disciplines and belong to the 2025 or 2026 batch are eligible.
2. Is this role open to freshers?
Yes. The Patient Safety Associate I position is an entry-level opportunity suitable for fresh graduates.
3. Where is the job location?
The position is based in Mohali, Punjab, India.
4. What is the application deadline?
According to the vacancy details, the deadline is 11 August 2026.
5. What skills are useful for this role?
Knowledge of ICSR processing, MedDRA coding, pharmacovigilance concepts, medical terminology, ICH guidelines, and Microsoft Office can strengthen your application.
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