This opportunity is suitable for fresh graduates from pharmacy, life sciences, and healthcare backgrounds who want to start their career in drug safety, adverse event reporting, and clinical safety operations.
Selected candidates will support global pharmacovigilance activities and work with safety data, regulatory documentation, and clinical safety processes.
Job Overview
| Particulars | Details |
|---|---|
| Position | Patient Safety Associate I |
| Company | Parexel |
| Location | Mohali, Punjab, India |
| Job Type | Full-Time |
| Experience | 0 - 1 years |
| Category / Department | Pharma |
| Application Mode | Online |
🏢 About Parexel
Parexel is a global clinical research organization (CRO) supporting pharmaceutical and healthcare companies in clinical development, regulatory services, and patient safety solutions.
The organization works on global healthcare projects and provides professionals opportunities to contribute to drug development, clinical research, and pharmacovigilance activities.
💡 Editor's Note / Preparation Tip
This recruitment update is created to help pharmacy and life science graduates explore entry-level opportunities in pharmacovigilance and patient safety. Candidates should verify job details, eligibility criteria, and application information through official company communication before applying.
📝 Job Description
Parexel Hiring Patient Safety Associate I | Pharmacovigilance Jobs 2026
Company Name: Parexel
Job Role: Patient Safety Associate I
Department: Pharmacovigilance / Drug Safety
Location: Mohali, Punjab, India
Employment Type: Full-Time
Experience: Freshers Preferred
Eligible Batch: 2025 & 2026 Graduates
Application Deadline: 02 July 2026
Eligibility Criteria
Candidates should have any of the following qualifications:
• PharmD
• M.Pharmacy
• Master’s Degree in Life Sciences
• BDS
Eligible Graduating Years:
• 2025
• 2026
Preferred Experience
Freshers are encouraged to apply.
Candidates with academic or internship exposure in:
• Pharmacovigilance
• Clinical Research
• Drug Safety
• Hospital Pharmacy
will have an advantage.
Salary Details (Estimated)
Expected salary range:
₹4.5 LPA – ₹6.5 LPA
Actual compensation may vary depending on qualification, skills, and company policies.
Why Join Parexel?
• Opportunity to enter the global pharmacovigilance industry
• Exposure to international safety projects
• Structured training programs
• Career growth in clinical research and drug safety
• Opportunity to work with global healthcare teams
• Experience with innovative therapies and patient safety initiatives
• Professional learning environment
How to Apply
Interested candidates can apply through the official Parexel recruitment process.
Applicants should highlight:
• Pharmacy / Life Science qualification
• Pharmacovigilance knowledge
• Clinical research exposure
• Relevant internships or projects
Begin your pharmacovigilance career with Parexel and contribute to improving patient safety worldwide.
🎯 Key Responsibilities
- ✓ Process Individual Case Safety Reports (ICSRs) from different sources
- ✓ Review and assess adverse event information
- ✓ Perform MedDRA coding for adverse events and medical history
- ✓ Prepare and review case narratives
- ✓ Conduct literature screening for safety information
- ✓ Support regulatory safety reporting activities
- ✓ Assist in safety surveillance and signal detection activities
- ✓ Follow pharmacovigilance regulations and SOP requirements
- ✓ Participate in quality checks and reconciliation activities
- ✓ Support aggregate safety report preparation
- ✓ Maintain safety tracking records and timelines
- ✓ Assist with audits and regulatory inspections
- ✓ Coordinate with internal teams and global stakeholders
💡 Required Qualifications & Skills
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This Patient Safety Associate I role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.
Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.
Expected Technical & Behavioral Questions:
- Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles. - Q2: What steps do you take when a quality deviation is detected in a product batch?
Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action). - Q3: How do you manage safety protocols while handling toxic chemicals?
Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
- Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
- Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated compensation for this role type in India is ₹2,40,000 - ₹3,80,000 per annum (Fresher analyst). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.
Frequently Asked Questions
Q1: Who can apply for the Parexel Patient Safety Associate role?
Candidates with PharmD, M.Pharm, Master’s in Life Sciences, or BDS qualifications can apply.
Q2: Are freshers eligible?
Yes, 2025 and 2026 graduates are encouraged to apply.
Q3: What field does this role belong to?
This role belongs to Pharmacovigilance and Drug Safety.
Q4: Is MedDRA knowledge required?
Basic awareness of MedDRA coding and adverse event reporting is preferred.
Q5: Where is the job location?
The position is based in Mohali, Punjab.
Q6: What career opportunities can follow this role?
Professionals can grow into roles such as Drug Safety Associate, PV Specialist, Safety Scientist, and Clinical Safety roles.
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