Clinical Research Associate

Employer Industry: Clinical Research and Healthcare Intelligence

• Competitive salary with additional benefits focused on well‑being and work‑life balance
• Opportunity for career advancement and growth within a reputable organization
• Flexible working environment with various annual leave entitlements
• Comprehensive health insurance offerings to suit personal and family needs
• Access to a Global Employee Assistance Programme for support and well‑being
• Inclusive and diverse workplace culture that values high performance and nurtures talent

• Conduct site qualification, initiation, monitoring, and close‑out visits for clinical trials
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process
• Collaborate with investigators and site staff to facilitate smooth study conduct
• Perform data review and resolve queries to maintain high‑quality clinical data
• Contribute to the preparation and review of study documentation, including protocols and clinical study reports

• Bachelor's degree in a scientific or healthcare‑related field
• Minimum of 12 months onsite monitoring experience as a Clinical Research Associate (CRA I, CRA II, or Senior CRA)
• In‑depth knowledge of clinical trial processes, regulations, and ICH‑GCP guidelines
• Strong organizational and communication skills with attention to detail
• Ability to travel at least 60% of the time (international and domestic) and possess a valid driver's license

• Experience working in a fast‑paced environment
• Proficiency in clinical trial management systems and electronic data capture
• Familiarity with regulatory submission processes
• Additional certifications related to clinical research

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