Participates in authoring and reviewing documents related to clinical trial safety, post-marketing safety, regulatory submissions and labeling
Job Summary
Participates in authoring and reviewing documents related to clinical trial safety, post-marketing safety, regulatory submissions and labeling.
Supports and provides oversight to staff involved in monitoring safety during clinical trials, including providing input on study protocols, statistical analysis plans and other clinical study-related documents, and performs data analysis to evaluate safety signals and interpret analysis results.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment.
Matching Summary
Participates in authoring and reviewing documents related to clinical trial safety, post-marketing safety, regulatory submissions and labeling.