Over +8 years, I've participated in more than 30 clinical trials involving Phase II,III and IV clinical studies.I am ultimately responsible for the successful management of investigator sites throughout the site life cycle, whilst working in accordance with ICH-GCP guidelines, the study protocol, applicable local and international regulatory requirements and internal Standard Operating Procedures. In addition to planning and conducting various site visits (feasibility, site selection, monitoring and close-out visit) in accordance with the clinical monitoring plan.
Contact Details
Tags
textile dictionary for translationsclinical trials in turkey
We鈥檝e updated our privacy policy so that we are compliant with changing global privacy regulations and to provide you with insight into the limited ways in which we use your data.
You can read the details below. By accepting, you agree to the updated privacy policy.
