Eccentric Clinical Research Private Limited is hiring an experienced Clinical Research Associate (CRA) in Gandhinagar, Gujarat. This opportunity is ideal for professionals with 2–3 years of clinical trial monitoring experience and strong knowledge of ICH-GCP guidelines, CDSCO regulations, and clinical operations.
If you are seeking a CRA job in India with hands-on site monitoring exposure, regulatory compliance experience, and career growth in clinical research, this role offers a dynamic and performance-driven environment.
About the Company
Eccentric Clinical Research Private Limited is a growing Clinical Research Organization (CRO) expanding its Clinical Operations team. The company focuses on protocol compliance, data integrity, regulatory excellence, and patient safety across clinical trials in India.
Job Overview – Clinical Research Associate (CRA)
- Position: Clinical Research Associate (CRA)
- Location: Gandhinagar, Gujarat
- Experience Required: 2–3 Years
- Qualification: B.Pharm / M.Pharm / Life Sciences (Bachelor’s/Master’s)
- Industry: Clinical Research / CRO
This CRA job involves end-to-end clinical trial monitoring, site management, and regulatory coordination aligned with ICH-GCP and CDSCO guidelines.
Key Responsibilities
The selected Clinical Research Associate will:
- Conduct feasibility assessments, Site Initiation Visits (SIVs), Site Monitoring Visits (SMVs), and Close-Out Visits (COVs).
- Ensure sites remain audit- and inspection-ready in compliance with ICH-GCP.
- Monitor patient recruitment, source data verification (SDV), and SAE reporting.
- Maintain and update Trial Master File (TMF/eTMF).
- Prepare regulatory and ethics submissions as per CDSCO requirements.
- Review protocols, ICFs, lab manuals, and eCRFs.
- Support Project Managers with monitoring plans and trial communication.
- Coordinate investigator payments, vendor payments, and study material logistics.
- Assist in investigator meetings and clinical training sessions.
- Contribute to SOP development and CAPA preparation.
- Ensure proper archival of study documents.
- Mentor junior CRAs and CTAs.
This role requires frequent travel for site visits and strong site management skills.
Required Qualifications & Skills
To qualify for this Clinical Research Associate job, candidates must have:
- Bachelor’s or Master’s degree in Life Sciences, B.Pharm, or M.Pharm.
- 2–3 years of CRA / Clinical Trial Monitoring experience.
- Strong understanding of ICH-GCP guidelines.
- Knowledge of CDSCO regulations and Indian clinical trial compliance.
- Excellent communication and documentation skills.
- Ability to manage multiple clinical sites and meet regulatory timelines.
- Strong problem-solving and organizational capabilities.
Why Apply for This CRA Job?
- Competitive salary package (₹5.5–7.5 LPA estimated range).
- Exposure to regulatory submissions and inspection readiness.
- Opportunity to work in a growing CRO environment.
- Hands-on experience in clinical monitoring and site management.
- Career growth in clinical operations and regulatory affairs.
How to Apply
Interested candidates can share their updated CV at:
📧 annushree.pv@eccentriccr.com