KCR
Clinical Monitoring • Functional Service Provider • Site Set up and Contracting • Late Phase • Medical & Regulatory Affairs
Clinical Research Associate I, II - Senior CRA
December 7
KCR
Clinical Monitoring • Functional Service Provider • Site Set up and Contracting • Late Phase • Medical & Regulatory Affairs
Description
• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process • Collaborating with investigators and site staff to facilitate smooth study conduct • Performing data review and resolution of queries to maintain high-quality clinical data • Contributing to the preparation and review of study documentation, including protocols and clinical study reports
Requirements
• Degree in medicine, science, or equivalent • Min. 1 year of direct monitoring experience • Fluent in Local Languages and English (verbal and written) • Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines • Driver's license • Hands on knowledge of Good Documentation Practices • Demonstrated high level of monitoring skill with independent professional judgment
Benefits
• Various annual leave entitlements • A range of health insurance offerings to suit you and your family’s needs • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead • Global Employee Assistance Program • Country-specific flexible benefits
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