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Parexel Hiring Study Startup Associate in Bengaluru
🏢 Parexel
📍 Bengaluru
🧪 Clinical Research
📄 Site Activation
💼 1–6 Years
Parexel is hiring Study Startup Associates for its Bengaluru office.
This opportunity is ideal for professionals interested in Clinical Research, Study Startup, Site Activation, Regulatory Submissions, CTMS, and eTMF Operations.
📘 Career Guide: Latest Clinical Research Jobs
📋 Parexel Recruitment 2026 – Overview
- Position: Study Startup Associate
- Company: Parexel
- Location: Bengaluru, Karnataka
- Employment Type: Full-Time
- Industry: Pharmaceutical & Life Sciences
- Department: Research & Development
- Experience: 1–6 Years
- Openings: 10
💰 Estimated Salary: ₹5 – ₹11 LPA
📌 Key Responsibilities
- Manage feasibility assessments and site identification
- Prepare IRB / IEC / EC submission dossiers
- Track amendments and ethics approvals
- Coordinate study startup and site activation activities
- Review ICFs, translations, and amendments
- Maintain CTMS and eTMF documentation
- Act as SPOC for assigned sites and countries
- Support startup risk management activities
📚 Learn Clinical Research Basics: Clinical Research Career Guide
🎓 Eligibility Criteria
- Life Sciences
- Pharmacy
- Biotechnology
- Related Healthcare Fields
📌 Required Experience:
- Clinical Research
- Study Startup
- Site Activation
- Regulatory Affairs
📌 Required Skills:
- ICH-GCP Guidelines
- IRB / IEC Submission Process
- CTMS & eTMF Systems
- Veeva Vault Knowledge
- Oracle / Siebel Platforms
- Stakeholder Coordination
🎁 Why Join Parexel?
- Global CRO exposure
- Career growth in clinical operations
- International regulatory experience
- Hands-on CTMS & eTMF exposure
- Collaborative work culture
- Long-term pharmaceutical industry career opportunities
📚 Learn More About Clinical Careers: Healthcare Career Knowledge Hub
💡 Interview Tips
- Revise ICH-GCP and regulatory guidelines
- Prepare CTMS and eTMF workflow basics
- Understand IRB / IEC submission processes
- Practice stakeholder coordination scenarios
- Prepare clinical startup lifecycle concepts
- Be confident discussing site activation experience
📊 Clinical Research Interview Guide: Clinical Research Interview Preparation
📄 Resume Tips
- Highlight CTMS and eTMF experience clearly
- Add clinical startup and regulatory projects
- Mention IRB / IEC submission exposure
- Use ATS-friendly formatting
- Showcase coordination and documentation skills
- Include clinical systems knowledge prominently
📚 Career Guidance: Healthcare Knowledge Hub
🚀 Apply Now
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📌 Note Before You Apply:
Kindly read the complete job description carefully before applying. Ensure your experience in clinical research, study startup, and regulatory documentation aligns with the role requirements before proceeding.
Kindly read the complete job description carefully before applying. Ensure your experience in clinical research, study startup, and regulatory documentation aligns with the role requirements before proceeding.
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