Parexel Hiring Freshers for Patient Safety Associate I – Excellent Pharmacovigilance Career Opportunity
If you’re a recent graduate in Life Sciences, Pharmacy, PharmD, or Dental Sciences and looking to begin your professional journey in the pharmaceutical and clinical research industry, then this opportunity could be the perfect fit for you. 🚀
Global Clinical Research Organization (CRO) Parexel has announced openings for the role of Patient Safety Associate I at its India offices. The position offers an exciting entry point into the world of pharmacovigilance, drug safety, and clinical research.
With only a short time left before the application deadline, eligible candidates are encouraged to apply as soon as possible.
Job Details
| Particulars | Details |
|---|---|
| Company Name | Parexel |
| Position | Patient Safety Associate I |
| Job ID | R0000042958 |
| Location | Mohali & Hyderabad |
| Employment Type | Full-Time |
| Eligible Batch | 2025 & 2026 Graduates |
| Qualification | M.Pharm, PharmD, Life Sciences, BDS |
| Application Deadline | June 25, 2026 |
About Parexel
Parexel is one of the leading global Clinical Research Organizations that supports pharmaceutical, biotechnology, and medical device companies in bringing innovative treatments to patients worldwide.
The company provides end-to-end clinical development services, regulatory consulting, pharmacovigilance support, and market access solutions. With operations across multiple countries, Parexel has built a strong reputation for quality, innovation, and patient-focused healthcare solutions.
Working at Parexel offers professionals exposure to international projects, advanced technologies, and opportunities to collaborate with healthcare experts from around the globe.
Role Overview
As a Patient Safety Associate I, you will contribute to drug safety and pharmacovigilance operations by reviewing, processing, and maintaining safety information related to pharmaceutical products and clinical studies.
This role plays a vital part in ensuring that adverse events and safety concerns are identified, documented, and reported according to global regulatory requirements.
Fresh graduates interested in pharmacovigilance careers will gain valuable hands-on exposure to safety databases, case processing, regulatory reporting, and quality management systems.
Key Responsibilities
Selected candidates will be responsible for the following activities:
📌 Safety Case Processing
- Review and process Individual Case Safety Reports (ICSRs).
- Enter safety data into pharmacovigilance databases.
- Perform medical coding using MedDRA terminology.
- Draft clinical narratives and conduct quality reviews.
📌 Literature Surveillance
- Conduct literature searches to identify adverse drug reactions.
- Monitor scientific publications for emerging safety information.
- Support signal detection activities.
📌 Regulatory Compliance
- Assist with safety submissions to health authorities and ethics committees.
- Ensure compliance with pharmacovigilance regulations and reporting timelines.
- Follow company SOPs and global guidelines.
📌 Data Management
- Maintain accurate and complete safety documentation.
- Resolve data discrepancies and support reconciliation activities.
- Coordinate follow-up information collection when required.
📌 Reporting & Metrics
- Support preparation of aggregate safety reports.
- Track compliance metrics and safety performance indicators.
- Assist senior team members in generating regulatory reports.
📌 Quality & Audit Support
- Participate in internal quality reviews.
- Assist during audits and inspections.
- Contribute to continuous process improvement initiatives.
Educational Qualification
Candidates must possess any of the following qualifications:
Eligible Degrees
✅ Master’s Degree in Life Sciences
✅ Master of Pharmacy (M.Pharm)
✅ Doctor of Pharmacy (PharmD)
✅ Bachelor of Dental Surgery (BDS)
Eligible Graduation Batch
- 2025 Pass-Out Candidates
- 2026 Pass-Out Candidates
Skills Required
To succeed in this role, candidates should possess:
Technical Skills
- Basic understanding of Pharmacovigilance concepts.
- Knowledge of ICH guidelines and drug safety regulations.
- Familiarity with MedDRA terminology.
- Proficiency in Microsoft Office applications.
Soft Skills
- Strong analytical thinking.
- Excellent attention to detail.
- Effective communication skills.
- Time management and multitasking abilities.
- Ability to work collaboratively in team environments.
Preferred Qualifications
Although freshers are welcome to apply, candidates with any of the following may receive additional consideration:
- Pharmacovigilance internships
- Clinical research training
- Drug safety certification programs
- Healthcare industry exposure
- Regulatory affairs experience
Why Start Your Career in Pharmacovigilance?
Pharmacovigilance has emerged as one of the fastest-growing sectors within the pharmaceutical and healthcare industry. As regulatory requirements become more stringent worldwide, the demand for trained drug safety professionals continues to increase.
Benefits of a Pharmacovigilance Career
✔ High industry demand
✔ Global career opportunities
✔ Strong salary growth potential
✔ Opportunities in CROs and pharmaceutical companies
✔ Exposure to international regulatory frameworks
✔ Contribution to patient safety and public health
For life science and pharmacy graduates, pharmacovigilance offers a stable and rewarding long-term career path.
Selection Process
The recruitment process may include:
- Application Screening
- Online Assessment (if applicable)
- HR Interview
- Technical Interview
- Final Selection
Candidates should keep their resumes updated and be prepared to discuss pharmacovigilance fundamentals during interviews.
How to Apply?
Interested candidates should submit their applications before the deadline.
Application Steps
1️⃣ Prepare an updated resume.
2️⃣ Highlight internships, projects, certifications, and relevant academic achievements.
3️⃣ Complete the online application form through Parexel Careers.
4️⃣ Review all details carefully before submitting.
⏳ Last Date to Apply: June 25, 2026
Early applications are strongly recommended as hiring processes may close once sufficient applications are received.
Final Thoughts
Parexel’s Patient Safety Associate I opening presents an outstanding opportunity for 2025 and 2026 graduates seeking a career in pharmacovigilance and clinical research. With exposure to global drug safety operations, regulatory reporting, and patient-focused healthcare initiatives, this role can serve as a strong foundation for long-term growth in the pharmaceutical industry.
If you meet the eligibility requirements and are eager to begin your journey in drug safety, don’t miss this opportunity. Apply before the deadline and take your first step toward a rewarding healthcare career. 🌟
🔗 Related Job Opportunities
- IKS Health Mega Recruitment 2026 | Bulk Openings for Certified Freshers & Experienced Medical Coders
- Sekhmet Pharmaventures Recruitment 2026 | Optimus Drugs Unit-3 Hiring Freshers & Experienced Candidates
- HAB Pharmaceuticals Recruitment 2026 | Multiple Openings in QA, QMS & Documentation
- Regulatory Affairs Executive Job Opening in Ahmedabad 2026 | B.Pharm Candidates Apply Now
- Mega Pharma Hiring Drive 2026 | Multiple Openings Across Maharashtra for Freshers & Experienced Candidates
