Veeda CR is a globally recognized clinical research organization (CRO) with a strong reputation for delivering high-quality clinical trial services. With 3.8/5 ratings from employees, Veeda CR is known for its adherence to ICH-GCP guidelines, robust regulatory compliance, and commitment to advancing clinical research.
Key Responsibilities
As a Clinical Research Associate (CRA), your role will include:
✅ Pre-Study & Site Management
- Conduct feasibility and site selection visits
- Ensure investigational sites meet study requirements
- Assist in regulatory submissions & contract management
✅ Clinical Trial Monitoring
- Perform on-site & remote monitoring visits
- Verify source data vs. eCRF entries
- Ensure ICH-GCP & protocol compliance
✅ Compliance & Documentation
- Maintain Investigator Site Files (ISF)
- Track drug accountability & safety reporting
- Ensure timely IEC/IRB submissions
✅ Investigator & Patient Safety
- Train investigators on study protocols
- Verify informed consent process
- Monitor adverse event (AE/SAE) reporting
✅ Audit & Financial Coordination
- Support regulatory inspections & audits
- Assist in investigator payment processing
Eligibility Criteria
Education:
- UG: B.Pharma / B.Sc in any specialization
- PG: M.Pharma / M.Sc in any specialization
Experience:
- 2-4 years in clinical research monitoring
- Strong knowledge of ICH-GCP guidelines
Why Join Veeda CR?
✔ Work from Home (Remote Opportunity)
✔ Competitive Salary (6-10 LPA)
✔ Global Exposure in Clinical Research
✔ Career Growth & Learning Opportunities
How to Apply?
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