Korea Pharma Solutions Clinical Research Associate I/II

• 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

• Bachelor's degree in a scientific or healthcare-related field. • 1+ year of SIT Oncology on-site monitoring CRA experience • Or 2+ years of SIT on-site monitoring CRA 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.

• For more details, please refer to the company website.