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Clinical Research Associate (CRA)
KGS Technology Group, Inc
United States
Not Disclosed
3 - 5 Years
Full Time - Permanent
Views:22
Applicants:3
Posted on 21 Aug, 2026
Remote
Job Description | Responsibilities
- Monitor clinical trials and ensure compliance with study protocols and GCP guidelines
- Coordinate with investigators, hospitals, sponsors and clinical research teams
- Conduct site visits, review patient records and verify clinical trial data
- Maintain trial documentation, reports and regulatory records
- Identify protocol deviations, support audits and ensure timely study completion
Overview
- Industry - IT - Consulting Services / Advisory Services
- Job Role - Clinical Research Associate (CRA)
- Employment type - Full Time - Permanent
- Work Mode - Remote
Qualifications
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
Clinical Research
Clinical Trials
GCP
Site Monitoring
Regulatory Compliance
Trial Documentation
Data Management
Pharmacovigilance
Medical Research