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Hiring Initiation Clinical Research Associate I (iCRA)
🏢 Parexel
📍 Bengaluru
📑 Clinical Start-Up
💊 Clinical Research
🌍 Global CRO
Parexel is hiring Initiation Clinical Research Associate I (iCRA) in Bengaluru for candidates interested in clinical trial start-up, regulatory submissions, CTMS management, and site activation activities.
This is an excellent opportunity for professionals looking to build careers in Clinical Operations, Clinical Trial Start-Up, Regulatory Affairs, Site Activation, and CRO Operations.
📅 Last Date to Apply: 15 May 2026
📘 Career Guide: Clinical Research Coordinator Career Guide
📋 Parexel Recruitment 2026 – Overview
- Position: Initiation Clinical Research Associate I (iCRA)
- Company: Parexel
- Location: Bengaluru
- Employment Type: Full-Time
- Industry: Clinical Research / CRO
- Experience: Clinical Research or Start-Up Experience Preferred
- Last Date: 15 May 2026
💰 Estimated Salary: ₹6.5 – ₹10 LPA
📌 Key Responsibilities
- Manage site activation and pre-SIV activities
- Handle IRB/IEC submissions and approvals
- Coordinate CDA and CSA documentation
- Conduct remote Qualification Visits (QVs)
- Maintain Trial Master File (TMF)
- Update Clinical Trial Management Systems (CTMS)
- Support regulatory submissions and amendments
- Build relationships with investigators and site staff
- Resolve compliance and training issues
📚 Learn More About TMF & Clinical Documentation: Clinical Documentation & CDISC Guide
💻 Required Skills
- Clinical trial start-up knowledge
- CTMS & eTMF systems exposure
- Regulatory submission understanding
- Strong analytical & problem-solving skills
- Stakeholder management abilities
- Communication and coordination skills
- Attention to detail & time management
- Knowledge of ICH-GCP guidelines
🧠 Practice Here: Clinical Trial Assistant Quiz
🎓 Eligibility Criteria
- Degree in Life Sciences
- Pharmacy
- Nursing
- Healthcare or Related Field
- Clinical Research Experience Preferred
- Knowledge of IRB/IEC Processes
🎁 Why Join Parexel?
- Work with a global CRO leader
- Exposure to international clinical trial processes
- Career growth in clinical operations
- Opportunity to specialize in start-up activities
- Collaborative work culture
- Experience with global regulatory systems
📚 Career Learning: Clinical SAS vs Clinical Data Guide
❓ Frequently Asked Questions
- Is prior CRA experience mandatory? Clinical research or start-up experience is preferred.
- What systems are used? CTMS and eTMF systems.
- Which city is the role located in? Bengaluru.
- What guidelines should candidates know? ICH-GCP and regulatory submission processes.
- What type of work is involved? Site activation, TMF management, and clinical start-up activities.
🧠 Prepare Before Applying
🚀 Job Application Link
📌 Important Note Before You Apply:
Please make sure to read the complete job description carefully before submitting your application. Make sure your qualifications and experience align with the role requirements before proceeding.
Please make sure to read the complete job description carefully before submitting your application. Make sure your qualifications and experience align with the role requirements before proceeding.
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