The responsibilities of the Clinical Research Associate include, but are not limited to:• Act as the main line of communication between the sponsor and the investigator• Verifying that all research staff, facilities and investigational products have adequate qualifications and resources and these remain adequate throughout• Responsible for the safety and proper conduct throughout the trial• Verifying that the investigator follows the approved protocol and all GCP procedures• Verifying that source data/documents and other trial records are accurate, complete, and maintained• Adverse events, concomitant medications, and inter current illnesses are reported in accordance with the protocol on the CRFs• Experience should include monitoring skills. Prior relevant active independent field monitoring experience and site management experience

2 years + CRA experience.

oncology study experience.