The Regulatory Start Up Associate I/II supports clinical trial site initiation and maintenance by pr
岗位职责
The Regulatory Start Up Associate I/II is responsible for supporting the initiation and maintenance of clinical trial sites, focusing on regulatory and start-up activities.
This role involves preparing, reviewing, and submitting regulatory documents to ethics committees and health authorities, ensuring compliance with local and international regulations.
The associate will coordinate with sites to collect essential documents, track submission timelines, and maintain accurate regulatory files.
申请条件
Bachelor's degree in life sciences, nursing, or a related field.
0-2 years of experience in clinical research, regulatory affairs, or a related area.
Knowledge of ICH-GCP guidelines and local regulatory requirements.
Strong written and verbal communication skills.
雇主简介
Novotech is a global clinical research organization (CRO) providing clinical trial services to biopharmaceutical companies. It offers structured graduate programs to train new professionals in clinical research.