Patrick Deji

Senior Clinical Research Associate @PSI CRO

Houston, TX, US

Performed pre‐site screening, site initiation, interim monitoring and close out visits for prospective, multi-center, clinical trials Trained clinical investigators and study staff to study protocol and appropriate federal regulations governing clinical trials Collaborated with study staff on developing and implementing corrective actions upon discovery of study compliance issues Assisted in protocol review processPrepared and conducted all site visits including, but not limited to, qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and close-out visits according to Biorasi’s SOPsIdentified potential centers for proposed studies in conjunction with the Project Team, and conducted feasibility assessment of sites as requiredEnsured that investigator site files are assembled appropriately and that all require documentation were in place, tracked and reconciled on a regular basis against the TMF filesSupported in mentoring less experienced CRAs on project or department tasks and requirementsPerformed other duties as required by the Department or Project TeamPerformed source document verification, retrieved Case Report Forms (CRFs) and performed query resolution in a timely manner and oversaw drug accountability and safety at investigative sitesEnsured Serious Adverse Event (SAE) reporting according to project specificationsResponded to requests from investigative sites in a timely manner.