Eric Psencik Email & Phone Number

San Antonio, Texas Area

San Antonio, Texas Metropolitan Area

San Antonio, Texas Area

• Coordinates and examines varying types of data from multiple sources for accuracy and consistency within protocol requirements; in accordance with Good Clinical Practices and sponsor requirements• Reports to the Institutional Review Board (IRB) the status of each study, creates annual reports for assigned studies, Serious Adverse Event (SAE) reports, deviations, violations and waivers from the protocol • Maintains all regulatory binders in compliance with FDA regulations, Good… Show more • Coordinates and examines varying types of data from multiple sources for accuracy and consistency within protocol requirements; in accordance with Good Clinical Practices and sponsor requirements• Reports to the Institutional Review Board (IRB) the status of each study, creates annual reports for assigned studies, Serious Adverse Event (SAE) reports, deviations, violations and waivers from the protocol • Maintains all regulatory binders in compliance with FDA regulations, Good Clinical Practices and sponsor requirements• Schedules and attends monitoring visits and resolves any outstanding issues Show less

San Antonio, Texas Area

• Collaborated with sponsor representative during entire duration of clinical trial, including monitoring on-site visits• Scheduled all aspects of subject visitations from outpatient care, dosing qualifications and medical procedures• Cataloged interim, annual and final reports to the Institutional Review Board (IRB) • Mentored new research associates, assistant research coordinators and research coordinators on integrity and quality of clinical research trials

San Antonio, Texas Area

• Maintained complete & accurate study related documents during the trial including FDA tables, Case Report Forms (CRFs) and source documentation• Oversaw 4-5 clinical studies per month with cohorts ranging between 6-120 subjects • Performed quality checks on source documents specific to study including flowcharts and Data Collection Sheets (DCS)• Responsible for entire clinical lab report process, including investigator assessment, repeats if necessary and filing of… Show more • Maintained complete & accurate study related documents during the trial including FDA tables, Case Report Forms (CRFs) and source documentation• Oversaw 4-5 clinical studies per month with cohorts ranging between 6-120 subjects • Performed quality checks on source documents specific to study including flowcharts and Data Collection Sheets (DCS)• Responsible for entire clinical lab report process, including investigator assessment, repeats if necessary and filing of labs• Served as supervisor of 5-6 person support staff after first period patient visitation Show less

San Antonio, Texas Area

• Worked with Recruitment Services Supervisor to instruct on protocol specific phone screening questionnaire and scheduling of potential volunteers to verify screening eligibility• Prepared study specific screening documentation and conducted individual screening recruitment visits• Reviewed medical history and necessary documentation with subjects in order to assess eligibility• Served as primary contact for subjects from screening period one check-in for in house studies to… Show more • Worked with Recruitment Services Supervisor to instruct on protocol specific phone screening questionnaire and scheduling of potential volunteers to verify screening eligibility• Prepared study specific screening documentation and conducted individual screening recruitment visits• Reviewed medical history and necessary documentation with subjects in order to assess eligibility• Served as primary contact for subjects from screening period one check-in for in house studies to handling subject eligibility, study specific questions, and concerns or events Show less