Regulatory Documents Jobs in China

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

1.    Supports the TA Head and Global TA Science Lead proposes development strategies and clinical pathways for new compound registrations in China.2.    Acts as China Local Clinical Leader to lead evidence generation working group for excellent delivery for trials in China and to assess new trial o...

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

Description Role Summary Responsibilities: You will be working on projects that involve the detailed analysis and creative presentation of clinical trial data for a range of clients including the industrys most successful pharmaceutical and medical technology companies patient and public health bodi...

(Senior) Clinical Research Physician represents frontline scientific expertisefor assigned AbbVie TA development in China. Provides clinical science insights on portfolio assessment developmental plan formation protocol discussion trial quality and safety oversight registration approval and life cyc...

Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenance activities.Essential Func...