Karl Sleem is a highly skilled Clinical Research Associate (CRA) with exceptional expertise in designing and managing clinical trials, ensuring their smooth implementation and monitoring them carefully throughout their duration. Karl holds a Bachelor's degree in Biochemistry, as well as a Master's degree in the same field, both from the prestigious American University of Beirut. With his extensive experience, Karl has become an expert in developing and writing trial protocols, presenting protocols to steering committees, designing data collection forms, coordinating with ethics committees, managing regulatory authority applications, and identifying/selecting suitable trial sites and investigators.

Karl's skill set includes liaising with doctors, consultants, or investigators on conducting clinical trials, setting up trial sites, monitoring trials throughout their duration, verifying data consistency, filing and collating trial documentation and reports, preparing final reports and sometimes manuscripts for publication, and archiving study documentation and correspondence. Karl is detail-oriented, ensuring all unused trial supplies are accounted for and closing down trial sites on completion of the trial.

Karl Sleem currently works as a CRA II at C.M.R.P.