Parexel Hiring Freshers for Pharmacovigilance – Patient Safety Associate I Job | Hyderabad & Mohali

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Parexel Hiring Freshers – Patient Safety Associate I | Pharmacovigilance Jobs 2026

Parexel

Hyderabad / Mohali

Freshers

Pharmacovigilance

Drug Safety

Full-Time

📄 About the Company

Parexel is a global Contract Research Organization (CRO) providing clinical development, pharmacovigilance, regulatory, and medical affairs services to leading pharmaceutical and biotech companies worldwide.

Parexel is known for its strong patient safety operations, global exposure, structured training, and long-term career growth in drug safety & pharmacovigilance.

📌 Job Overview

Parexel is hiring Patient Safety Associate I for its Hyderabad and Mohali offices.

This is a fresher-friendly entry-level pharmacovigilance role supporting global patient safety activities such as ICSR processing, literature review, regulatory reporting, and medical monitoring support.

This role is ideal for candidates looking to build a long-term career in Drug Safety / PV / Clinical Research.

🧪 Job Details – Patient Safety Associate I

Company: Parexel

Position: Patient Safety Associate I

Location: Hyderabad / Mohali

Experience: Freshers

Employment Type: Full-Time

Work Mode: Office-based / Hybrid (as per business requirement)

Domain: Pharmacovigilance / Patient Safety / Drug Safety

🧾 Key Responsibilities – Drug Safety Operations

• Assist in developing project-specific safety workflows, templates, and procedures
• Support safety database setup and User Acceptance Testing (UAT)
• Triage incoming safety case reports for completeness and validity
• Enter and review safety data in Pharmacovigilance databases
• Perform quality checks and ensure accurate ICSR processing
• Handle follow-up queries, MedDRA coding, and narrative writing
• Maintain case files, project documents, and safety tracking logs
• Support Medical Directors and Safety Physicians in medical monitoring tasks

📑 Regulatory & Pharmacovigilance Compliance

• Perform literature searches and document safety findings
• Support audit and regulatory inspection preparation
• Assist in expedited reporting and SUSAR unblinding activities
• Submit safety cases via global reporting systems (ISIS / E2B)
• Track regulatory submissions and compliance metrics
• Support global electronic reporting registrations

🎓 Educational Qualifications

• M.Pharmacy (Pharmacology / Pharmaceutics / Clinical Pharmacy)
• Pharm.D
• MSc in Pharmacovigilance / Clinical Research (2025 pass-outs preferred)
• BDS (Bachelor of Dental Surgery)
• Prior healthcare / clinical exposure is an added advantage

🧠 Required Skills

• Strong analytical and problem-solving skills
• Excellent written and verbal communication
• Good knowledge of computer applications and databases
• Ability to perform literature searches
• Strong organizational and prioritization skills
• Team-oriented mindset with client focus
• Ability to work in a global, process-driven environment

💼 Why Join Parexel?

• Hands-on exposure to global pharmacovigilance projects
• Structured training and continuous learning programs
• Strong career growth in patient safety & regulatory roles
• Work with cross-functional medical and regulatory teams
• Supportive and learning-driven work culture

📌 Note Before You Apply:
We use a 15-second timer to encourage candidates to read the job description carefully before applying. Please ensure your qualification aligns with Pharmacovigilance / Patient Safety requirements.

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