JOINN’s Clinical Operations Team boasts substantial hands-on experience in domestic and international clinical trials. Strictly adhering to ICH and GCP guidelines, the team supports diverse project types including multi-phase registrational trials for new drugs, bioequivalence (BE) studies, Investigator-Initiated Trials (IIT), real-world studies, and clinical research for biomedical technology translation under Decree No. 818.
With project managers serving as overall leads, the team oversees end-to-end project organization, coordination, timeline and quality management across the full workflow: project initiation and preparation, site management, subject recruitment and follow-up, through to database lock, study close-out and document handover.
All projects are led by a dedicated PM coordinating monitors, QA/QC, statistics, medical and regulatory teams for cross-functional alignment.
•Project management & monitoring for Phase I–IV new drug trials
•BE bioequivalence trial project management & monitoring
•IIT project management & monitoring
•Real-world research project management & monitoring
•Biomedical technology transformation trial management & monitoring
•Diverse cross-therapy project track record
•Closed-loop standardized operation SOPs
•Single-point PM oversight for all clients
•Multi-scenario adaptive execution capacity
•Dual control of quality & timeline
Project manager organizes, coordinates, manages and controls the progress and quality of the project throughout the whole lifecycle.
