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Parexel Hiring Initiation Clinical Research Associate I (iCRA) in Bengaluru
🏢 Parexel
📍 Bengaluru
🧪 Clinical Research
📑 Site Activation
💻 CTMS / eTMF
Parexel is hiring for the role of Initiation Clinical Research Associate I (iCRA) in Bengaluru, India.
This opportunity is ideal for candidates with experience in clinical trial start-up activities, regulatory submissions, CTMS management, site activation, IRB submissions, and TMF documentation.
📋 Job Overview
🏢 Company: Parexel
💼 Position:
Initiation Clinical Research Associate I (iCRA)
📍 Location:
Bengaluru, India
🧑💻 Experience Required:
2–4 Years
🎓 Qualification:
Degree in Life Sciences, Pharmacy, Nursing, Healthcare, or related fields
🏭 Industry:
Clinical Research / CRO / Clinical Operations
💰 Estimated Salary: ₹6.5 – ₹10 LPA
📌 Key Responsibilities
🧪 Clinical Trial Start-Up Activities
- Manage site activation and pre-SIV activities
- Handle IRB/IEC submissions and approvals
- Coordinate CDA and CSA documentation
- Conduct remote Qualification Visits (QVs)
📑 Regulatory & Documentation Management
- Prepare and submit ICFs and amendments
- Maintain Trial Master File (TMF)
- Ensure CTMS updates with First Time Quality
- Manage clinical start-up documentation
🤝 Site & Stakeholder Management
- Act as primary contact for trial sites
- Build relationships with investigators and site staff
- Resolve compliance and timeline-related site issues
✅ Compliance & Quality
- Ensure adherence to ICH-GCP guidelines
- Maintain audit and inspection readiness
- Monitor protocol compliance and data quality
🎓 Eligibility & Required Skills
- Bachelor’s degree in Life Sciences, Pharmacy, Healthcare, Nursing, or related field
- Experience in clinical research or start-up activities
- Knowledge of IRB/IEC processes
- Understanding of CTMS and eTMF systems
- Strong communication and stakeholder management skills
- Problem-solving and analytical abilities
- Attention to detail and time management
🌍 Why Join Parexel?
- Work with a global CRO leader
- Exposure to international regulatory processes
- Career growth in clinical operations
- Opportunity to become a clinical start-up specialist
- Collaborative and high-performance work culture
- Experience with global clinical trial projects
📄 Resume Tips for CRA Roles
- Highlight CTMS, TMF, and IRB submission experience
- Add clinical trial and GCP knowledge clearly
- Mention start-up and site activation activities
- Use ATS-friendly keywords for clinical research roles
- Keep resume concise and achievement-focused
🎯 Interview & Preparation Resources
👉 Aptitude & Reasoning Quiz
👉 Interview Questions & Preparation
👉 Explore More Healthcare Quizzes
💡 Interview Tips
- Prepare basics of ICH-GCP and clinical trial phases
- Understand IRB/IEC and regulatory submission processes
- Revise CTMS, eTMF, and TMF concepts
- Be ready to explain start-up workflows and timelines
- Demonstrate communication and problem-solving skills
🧩 Fun Learning & Career Growth
🚀 Job Application Link
📌 Important Note Before You Apply:
Please make sure to read the complete job description carefully before submitting your application. Understanding the role and responsibilities increases your chances of getting shortlisted.
Please make sure to read the complete job description carefully before submitting your application. Understanding the role and responsibilities increases your chances of getting shortlisted.
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