A leading clinical research opportunity is now open for an experienced Clinical Research Associate (CRA) in Ahmedabad. CurexBio is hiring a skilled CRA with approximately 3 years of experience in clinical trial monitoring and strong knowledge of ICH-GCP guidelines and regulatory compliance.
This Clinical Research Associate job in Ahmedabad is ideal for professionals with hands-on experience in Phase I–IV clinical trials, site management, and regulatory documentation. If you are looking to grow your career in clinical research and clinical trial operations, this role offers strong exposure and advancement potential.
Job Overview
- Position: Clinical Research Associate (CRA)
- Location: Ahmedabad (Onsite)
- Experience: ~3 Years as CRA
- Education: Bachelor’s or Master’s in Science
- Industry: Clinical Research / Pharmaceutical
Key Responsibilities – Clinical Research Associate
The selected candidate will:
- Monitor Phase I–IV clinical trials across assigned sites
- Ensure compliance with ICH-GCP guidelines and regulatory requirements
- Conduct site initiation, monitoring, and close-out visits
- Review essential documents and maintain Trial Master File (TMF) accuracy
- Verify source data and ensure protocol adherence
- Coordinate with investigators and site staff
- Track timelines, enrollment, and data quality metrics
- Prepare monitoring reports and regulatory documentation
- Manage multiple sites and ensure inspection readiness
This Clinical Research Associate job requires strong documentation skills, regulatory understanding, and the ability to handle multiple timelines efficiently.
Qualifications & Requirements
- Bachelor’s or Master’s degree in Science (Life Sciences preferred)
- Approximately 3 years of experience as a Clinical Research Associate
- Strong knowledge of ICH-GCP and regulatory guidelines
- Experience handling Phase I–IV clinical trials (preferred)
- Excellent communication and documentation skills
- Ability to manage multiple clinical trial sites
- Willingness to travel as required
Preferred Skills
- Site management experience
- Audit and inspection readiness exposure
- Risk-based monitoring understanding
- Regulatory submission coordination
Salary & Benefits
- Estimated Salary Range: ₹6,00,000 – ₹9,00,000 per annum
- Opportunity to work on multi-phase clinical trials
- Professional growth in clinical operations
- Exposure to regulatory compliance and global standards
How to Apply
Interested candidates can share their updated CV at: