Clinical Research Associate

To support the successful delivery of clinical trials, the full-time Clinical Research Associate will manage site qualification, monitoring, and close-out visits while ensuring patient safety and data quality in a hybrid work environment. Key Responsibilities Conduct site qualification, initiation, monitoring, and close-out visits in accordance with study protocols and regulations Ensure subject safety, data integrity, and protocol compliance throughout the study lifecycle Build and maintain strong relationships with investigators, study coordinators, and site personnel Required Qualifications Bachelor's degree in Life Sciences or a related field 3-4 years of Clinical Research Associate experience within the pharmaceutical, biotechnology, or CRO industry Solid understanding of ICH-GCP, clinical trial processes, and applicable regulations Demonstrated ability to work independently and take ownership of site activities and deliverables Oncology and/or Phase I clinical trial experience is preferred but not essential