Parexel Hiring Initiation Clinical Research Associate I (iCRA) – Bangalore | Clinical Start-Up Role

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Parexel Hiring Initiation Clinical Research Associate I (iCRA) – Bangalore | Clinical Start-Up Role

✔ Verified by Medical Jobs India

Hiring Initiation Clinical Research Associate I (iCRA) 

🏢 Parexel
📍 Bangalore
🎓 Life Sciences / Pharmacy / Nursing
💼 Clinical Research

Parexel is hiring Initiation CRA (iCRA) for clinical trial start-up activities including site activation, IRB submissions, and TMF management.

👉 Understand clinical research roles: Clinical Research Career Guide

🎯 Practice before applying: Clinical Trial Assistant Quiz

📋 Job Overview

  • Role: Initiation Clinical Research Associate I
  • Company: Parexel
  • Location: Bengaluru
  • Experience: Clinical research / start-up experience
  • Job Type: Full-Time
  • Salary: ₹6.5 – ₹10 LPA (Estimated)
  • Last Date: 08 May 2026

📌 Key Responsibilities

  • Manage site activation and start-up activities
  • Handle IRB/IEC submissions
  • Coordinate CDA & CSA agreements
  • Conduct qualification visits (QVs)
  • Maintain Trial Master File (TMF)
  • Ensure CTMS updates
  • Build relationships with clinical sites
  • Ensure compliance with ICH-GCP

📘 Learn data & systems: Clinical Data vs SAS

📊 CDISC basics: CDISC Guide

🎯 Required Skills

  • Clinical trial start-up knowledge
  • CTMS & eTMF systems
  • Regulatory submission experience
  • Problem-solving & analytical skills
  • Stakeholder communication
  • Time management

🧠 Improve skills: Interview Questions

🎓 Qualifications

  • Bachelor’s degree in Life Sciences / Pharmacy / Nursing
  • Clinical research or start-up experience
  • Knowledge of IRB/IEC processes

🌟 Benefits

  • Work with global CRO leader
  • Exposure to international trials
  • Career growth in clinical operations
  • High learning environment

🚀 Job Application Link

📌 Important Note Before You Apply:

Kindly read the full job description carefully before applying. Ensure your profile aligns with clinical trial initiation, site activation, and clinical research monitoring requirements before proceeding.

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