Kenny Diricks

Clinical Research Associate with more than 13 years of experience as CRA with 3 years of experience as Co-Lead CRA / EU Project Manager.

Worked as both blinded and unblinded monitor on more than 50 clinical trials in different Therapeutic areas, including Cardiology/Vascular Diseases, Dermatology, Devices, Digestive, Endocrinology/Metabolic Diseases, Genitourinary, Hematology/Oncology, Infectious/Parasitic Diseases, Musculoskeletal, Nervous System, Ophthalmology, Rare/Genetic diseases/Disorders and Respiratory. 

Gained significant experience in Hematology/Oncology and Nervous System Therapeutic areas as CRA.

Experience in Clinical trials phases I-IV, Observational and Registry studies in both adult and pediatric population. 

Performed all types of Monitoring Visits: PSV, SIV, IMV and COV. Participated in feasibilities activities.

Used different Clinical and client specific systems for trial management, such as EDC, CTMS, IVRS, IWRS, eDiaries. Performed 100% or reduced SDV, on-site and remote visits.

Familiar with AIM methodology and trained in Risk Based Monitoring.

MSc., Physical Therapy, 2003 (Provinciale Hogeschool Limburg, Limburg, Belgium)