Make clinical development plan and complete clinical trial protocol design
Review clinical trial documents, such as Case Report Form (CRF), Statistical Analysis Plan (SAP), Data Management Plan (DMP) and Drug Safety Report Management Plan and so on. Make sure these documents are completed before the deadline
Solve medical problems and analyze data related to medicine in clinical study. Make sure the clinical study conform to clinical trial protocol, ICH, GCP and company SOP
Engage with clinical specialists and drug regulatory authorities on clinical study design and development strategies and so on
Qualifications
Education: M.D, or MBBS
Language Requirement: Professional working proficiency in English