Regulatory Affairs-Office Based-South Korea ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies.

• 안전관리자료, 해외사용현황, 품질, 표시자재, 수입실적, 허가증 – 갱신 식약처 제출 업무 • SMF (Site Master File) - 해외제조소 (원료 수입처) 등록 관련 업무 • OTC (일반 의약품) 품목 신고 • DMF (Drug Master File) - 원료 의약품 등록

• Bachelor's degree in a scientific or healthcare-related field. • Prior experience or strong interest in clinical research. • Knowledge of clinical trial processes, regulations, and guidelines. • Excellent organizational and communication skills. • Ability to work collaboratively in a fast-paced environment with attention to detail.

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