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· Provide Chinese clinical strategy for NPI; Lead the clinical plans development to be compliance with GCP, the regulation, Philips harmonized clinical SOPs;
· As key scientific reviewer to assess the scientific and ethical of the company sponsor study & IIS;
You are responsible for
• Participate in the evidence generation processes for NPI & LCM
• Participate in the CDMA(Clinical Development and Market Access) process
• Participate in the development of clinical deliverables, including clinical evaluation reports, clinical trial protocols, CSRs & clinical sections of regulatory submissions
• Working closely with Clin Ops and BS&DM on day to day management of assigned clinical studies
• Supports clinical literature searches and reviews
These jobs might be a good fit