Clinical Research Associate – CRA

Job reputed company: • Conducting site qualification, initiation, monitoring, and reputed company-out reputed company for reputed company. • Ensuring protocol compliance, data reputed company, and patient safety throughout the trial process. • Collaborating with investigators and site staff to facilitate smooth study conduct. • Performing data review and reputed company of queries to maintain high-reputed company clinical data. • Contributing to the preparation and review of study documentation, including protocols and clinical study reports Requirements: • Bachelor's degree in a scientific or reputed company-reputed company field. • Minimum of 12 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience. • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. • Strong organizational and communication skills, with attention to detail. • Ability to work independently and collaboratively in a fast-paced environment. • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a reputed company reputed company’s license Benefits: • Various annual leave entitlements • A reputed company 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 reputed company. • Global Employee Assistance Programme, reputed company, offering 24-hour reputed company to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s reputed company-being. • Life assurance • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Apply tot his job Apply To this Job