You take responsibility for the administration and monitoring of clinical research projects according to our Standard Operating Procedures and the relevant guidelines. You analyze and evaluate clinical data, ensure compliance with protocol and overall clinical objectives; identify, select, initiate and close-out appropriate investigational sites for clinical studies. You monitor the sites in order to ensure that studies are carried out according to the applicable regulations and guidelines. Regular travel is required.
We are looking for CRA's in New York & Cleveland, USA
By preference, you have a (para-) medical or scientific degree and at least one (1) year of clinical research experience including monitoring, or at least a minimum of two years experience in pharmaceutical data management or as a study coordinator. You are a detail oriented professional with good negotiation, time management and people skills.
Fluent in English