Comprehensively manage, control quality, and supervise projects in accordance with the Drug Registration Regulations, GCP, and other relevant clinical trial regulations, ensuring timely and high-quality project delivery.
Provide guidance and oversee the execution of CRAs within the project team.
Assist department managers in improving departmental systems and upgrading SOPs, and support the smooth implementation of new systems.
Be responsible for CRA project-related training.
Manage project costs, control unnecessary expenses, and review CRA monitoring plans.
Externally coordinate relationships among research centers, sponsors, data management and statistical personnel, and maintain good communication.
Bachelor’s degree or above in medicine, biology, or related fields.
At least 3 years of clinical trial management experience in metabolic/endocrine or oncology projects.
Familiar with the Drug Registration Regulations, GCP guidelines, and other relevant regulations, and thoroughly understand the entire clinical research process.
Strong abilities in management, organization, coordination, and problem-solving.
Excellent skills in planning and execution.
High sense of responsibility and strong ability to work under pressure.