Worldwide Clinical Trials - APAC in Australia is seeking a professional for regulatory affairs to manage submissions, ensure compliance with ICH GCP guidelines, and maintain local documentation. The ideal candidate will possess a degree in related sciences, a minimum of three years' experience in clinical research, and skills in communication and organization. Proficiency in MS Office and knowledge of local regulatory environments are preferred. Join a diverse and innovative team dedicated to improving lives through clinical trials.#J-18808-Ljbffr