Full Time


Posted 1 month ago
Application ends: November 9, 2021
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Job Description



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


Strong knowledge in ICH-GCP

Ability to review and evaluate clinical data

Computer literacy desirable

Professional use of the English language; both written and oral

Good oral and written communication skills

Due to the nature of this position it may be required for the employee to travel

Bachelor degree, or local equivalent, in medicine, science or related discipline