Implement overall clinical project plans in accordance with ICH-GCP and study protocols.
Monitor project progress, budget, and quality against key timelines and milestones, assess related risks, and develop mitigation strategies.
Oversee the selection, evaluation, and quality control of clinical trial centers and CRO suppliers.
Participate in trial protocol design and discussions, and review critical clinical documents.
Maintain good relationships with research units and all clinical trial parties, coordinating to resolve any issues that arise.

Bachelor’s degree or higher in Clinical Medicine, Pharmacy, or related field.
Over 5 years of experience in clinical research implementation with a CRO or pharmaceutical company, including at least 2 years in project management. Experience in managing small molecule innovative oncology drug projects is preferred.
Proficiency in the entire clinical research process and understanding of regulatory policies.
Strong project management, communication, problem-solving skills, resilience, and execution ability.
Trustworthy, meticulous, rigorous, with a strong sense of responsibility and willingness to travel.