Corporate


John L. Capicchioni – Chief Commercial Officer


Mr. John L. Capicchioni brings 26 years of global CRO experience to the Cliantha Group of companies. He has held a broad range of executive leadership positions, overseeing global sales, project management, marketing, client services and operations. Mr. Capicchioni holds a Chemistry degree from Rutgers University.

Mr. Capicchioni is well-known in the industry for his leadership, integrity, energy and passion. With his strong strategic focus, understanding of the marketplace and commitment to all stakeholders, he assists Cliantha in providing a unique form of customer advocacy, emphasizing quality, accountability, timeliness and budget management in all aspects of our customer-focused clinical research initiatives and data management practice. He has also served on the board of directors of the leading Generic Pharmaceutical Association as the elected member for Contract Research Organizations.

Dr. Jorge Lujan-Zilbermann, M.D., Principal Investigator/Medical Director.


Dr. Lujan is Board Certified in Pediatrics and Pediatric Infectious Diseases as wells as an ACRP certified Principal Investigator. In Dr Lujan's 15 years of clinical research experience he has been involved in more than 100 clinical trials as Principal Investigator or Sub Investigator.

His experience includes Dermatology Trials, Medicated Patch Trials, Bioequivalence Studies, and Personal Healthcare studies. Dr. Lujan has worked on a range of dermatological conditions and diseases.

Madelaine Perez - Director of Clinical affairs and Operations.


Madelaine has been involved in the clinical research industry for over twenty years, assisting pharmaceutical, biotech and Clinical Research Organizations with designing, conducting and overseeing Phase I-IV clinical trials. She has engaged external therapeutic experts to build a robust clinical study TEAM.

Mrs. Perez works cross-functionally with external partners to select and modify clinical study designs to align with target markets and Agency objectives. She manages the approval, direction, planning, execution, interpretation of clinical trials/research, logistics, SOP development and the data collection activities in accordance with current Good Clinical Practices. Madelaine has a Doctorate in Bacteriology from the Metropolitan University of Colombia and a Masters in Behavioral Sciences. She has worked for the Department of Health for seven years in the Health Care, Food and Water Department and is classified as a level II Biological Scientist by the State of Florida.
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