Experior is in charge of the site management organization in order to help in the success of the ongoing clinical research. This is achieved through the introduction of qualified principal investigators, previously recruited from any therapeutic area, with access to a wide patient population for the study. Thanks to the study coordinators of Experior in the clinical site, who are highly qualified and with complete dedication, and who perform their activity at the investigational site, we achieve a fluid communication between the sponsor and the investigator, and we ensure an appropriate data collection within the deadlines.

• Capacity to offer several quality sites by a telephone call
• Capacity to coordinate studies from Phase I to Phase IV
• Capacity to coordinate hospital and outpatient studies
• Wide database of highly qualified investigators who are experienced and enthusiastic
• Clinical trial coordinators who work full time and have experience
• Full national coverage
• Access to wide patient populations with cultural diversity
• Efficient and centralized contractual and budget solutions
• Close work relationships with IEC/IRB and foundations
• Long-standing, stable relationships with a high number of public and private institutions
• In case of emergency, we provide sites within 72 hours through our fast recruitment process
• Optimization of patient recruitment to support the efforts of the local site
• Efficient, stable and beneficial work relationships with the investigational sites for both parties
• Unique and personalized services with clients that take part in our recruitment program