Patient Safety Associate I
Are you seeking high-paying Parexel Patient Safety Associate Jobs or Pharmacovigilance Fresher Jobs in Mohali? Global contract research leader, Parexel, is currently hiring for the position of Patient Safety Associate I based at its modern operational hubs in Mohali and Hyderabad, India.
This role is open exclusively for 2025 and 2026 pass-outs holding master's degrees in pharmacy or life sciences, as well as BDS and Pharm.D graduates. To optimize your registration on MNC career portals, check our complete guide on how to apply for healthcare and pharma jobs.
📋 Job Overview
| Particulars | Details |
|---|---|
| Position | Patient Safety Associate I |
| Company | Parexel (Leading Global CRO) |
| Locations | Mohali & Hyderabad, India |
| Employment Type | Full-Time |
| Experience Required | Freshers (2025 & 2026 Batches Only) |
| Educational Background | M.Pharm, B.Pharm, Pharm.D, BDS, M.Sc (Life Sciences, Biotech, Biochem, Micro) |
| Expected Salary | ₹3.5 LPA – ₹6.0 LPA (Estimated) |
| Application Deadline | June 25, 2026 (Apply Immediately) |
💼 Key Responsibilities
1. Pharmacovigilance & ICSR Processing
- Monitor and triage safety reports received through safety mailboxes, clinical literature, or EudraVigilance.
- Perform accurate data entry of individual case safety reports (ICSRs) into safety databases.
- Conduct clinical event coding using standard MedDRA dictionaries.
- Prepare Adverse Drug Reaction (ADR) reporting forms and compile medically coherent narratives.
- Identify missing data and follow up with clinical investigators to resolve database queries.
2. Safety Reporting & Global Compliance
- Coordinate safety submissions of expedited cases to regulatory authorities within strict timelines.
- Support QA review workflows and investigate case compliance metrics.
- Maintain comprehensive safety documentation and ensure real-time audit readiness.
3. Literature Review & Signal Detection
- Conduct systematic searches of medical literature databases to identify adverse events.
- Analyze clinical journals and extract drug safety information and safety signals.
- Perform peer review assessments of database search queries and literature outputs.
4. Regulatory & Affiliate Support
- Assist in drafting regulatory reports, including eCTD submissions, PBRERs, and Risk Management Plans (RMP).
- Support post-market lifecycle management and coordinate safety data exchange with global affiliates.
🎓 Qualifications & Skills Required
Candidates with the following qualifications are eligible to apply:
- Master of Pharmacy (M.Pharm) / Bachelor of Pharmacy (B.Pharm) / Pharm.D
- M.Sc in Life Sciences (Biotechnology, Biochemistry, Microbiology, or related disciplines)
- Bachelor of Dental Surgery (BDS) or equivalent clinical medical degrees
- Only 2025 and 2026 batch graduates are eligible for this fresher intake
For pharmacy post-graduates planning international safety careers, read our comparison on B.Pharm/M.Pharm Career Scope: India vs USA.
Core Competencies
- Basic understanding of drug safety operations, clinical trial phases, and ICH-GCP guidelines.
- Familiarity with pharmacovigilance databases and MedDRA terminology.
- Excellent written and verbal communication skills in English.
- Detail-oriented approach with strong analytical and problem-solving abilities.
If you want to verify your drug safety concepts prior to screening rounds, try our Entry Level Pharmacovigilance Quiz or test yourself with our Drug Safety Analyst Quiz.
💰 Compensation & Employee Benefits
Parexel provides competitive entry-level packages, including:
- Estimated Salary: ₹3.5 LPA – ₹6.0 LPA.
- Hands-on training in global safety databases and MedDRA coding systems.
- Exposure to global clinical trial safety workflows and regulatory frameworks.
- Continuous learning opportunities within a supportive CRO ecosystem.
- Fast-track career paths into Drug Safety Associate or Safety Scientist positions.
Safety professionals secure highly lucrative packages as they progress. Check our salary analysis on Pharmacovigilance Salary: India vs USA to learn about global earnings.
🌟 Why Join Parexel?
- Parexel is one of the world's largest, most respected clinical research organizations.
- Contribute directly to global patient safety and life-saving drug development.
- Excellent learning platforms to develop expertise in medical coding and case analysis.
If you want to review typical interview formats, read our database of the Top 100 Pharmacovigilance Interview Questions.
📑 Resume Tips
- Highlight any academic coursework, projects, or training in Pharmacovigilance.
- Mention your graduation year clearly (2025 or 2026) to confirm eligibility.
- List computer database proficiency, MS Excel skills, and medical terminologies.
- Ensure your CV is clean, professional, and ATS-compliant.
🎯 Interview Questions
- What is an Individual Case Safety Report (ICSR), and what are its four minimum criteria?
- What does MedDRA stand for, and how is it used in adverse event coding?
- How do you determine if a case requires expedited reporting to regulatory agencies?
- What is the difference between active surveillance and passive surveillance?
- Describe your understanding of the role of a Patient Safety Associate in clinical trials.
📌 How to Apply?
Interested and eligible freshers can apply online directly through Parexel's Workday recruitment portal. The deadline to submit applications is June 25, 2026. To prepare your profile and optimize your registration, read our guide on how to apply for healthcare and pharma jobs online.
🚀 Apply Now
Apply Online❓ Frequently Asked Questions
Q. When is the application deadline?
The portal closes on June 25, 2026. Interested candidates are advised to apply as early as possible.
Q. Can 2024 graduates apply?
Parexel has specified that this fresher intake is for 2025 and 2026 graduating batches only.
Q. What is the job location?
The role is primarily based at Parexel's operational offices in Mohali, Punjab with Hyderabad as a key hub.
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