Assist and ensure CRO personnel manage center setup, ethics submissions, ethics committee approvals, and contract negotiation guidance within project timelines.
Participate in organizing and attending investigator meetings and project initiation meetings.
Collaborate with CRO staff for comprehensive management of study centers, ensuring compliance with GCP, SOPs, study protocols, and Chinese laws and regulations, timely completion of site initiation, routine monitoring, and site closure.
Jointly complete high-quality site visit reports with CRO staff.
Assist in reporting AE/SAEs at study centers and follow-up.
Ensure patient safety and rights through consent verification.
Ensure data integrity and accuracy through source data verification and case report form/data query management.
Supervise study center trial materials, including drugs, documents, and related equipment.

Bachelor's degree or higher in Medicine or Pharmacy, clinical background preferred.
Independent work capability, strong communication, coordination, and persuasion skills.
Physically fit, outgoing, and communicative.
Computer proficient.
Open to frequent travel.
Over 2 years of relevant experience.
Ability to work independently and as part of a team; excellent verbal and written communication skills; proactive problem-solving related to project management.