北京招聘

Job overview

Supports compliance with protocol execution from a medical and scientific perspective

Provides medical expertise during project delivery lifecycles; 

Provides medical support to project teams and investigative sites; 

Clarifies protocols and inclusion/exclusion determinations; 

Advises around patient safety issues; 

Performs medical reviews and clarifications of trial-related and post marketing studies Adverse Events; 

Signal detection and aggregated reporting; and conducting project delivery lifecycles (premarketing and post marketing).

Experience

Typically requires 2 - 3 years of prior relevant experience.    

QuintilesIMS pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow us to create more effective trials and determine outcomes faster.
 
If that is your passion, we have a place for you.