CRA II based in Korea Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know:

• Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms • Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates • Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials • Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues • Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans • Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct

Qualifications: • Bachelor's degree in a related field or equivalent experience • Minimum of 2-4 years of experience in clinical research monitoring • Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements • Excellent communication and interpersonal skills • Ability to work independently and manage multiple priorities • Proficiency in using clinical trial management systems and other relevant software Certifications: • Certified Clinical Research Associate (CCRA) or equivalent certification preferred Necessary Skills: • Attention to detail and strong analytical skills • Problem-solving abilities and critical thinking • Ability to work effectively in a team environment • Strong organizational and time management skills • Proficiency in Microsoft Office Suite

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