Sasha Studebaker Email & Phone Number

San Diego, California, United States

Upland, California, United States

Adhered to Good Clinical Practices and specific study protocolsEnsured scientific integrity of data and protected the rights, safety, and well-being of patients enrolled in clinical trialsDiscussed study protocols with patients and verified the informed consent documentationEnsured patient’s referring physician receives notification of patient’s participation in studies as requested by the patientMet with patient for each visit and maintained accessibility to discuss any questions or concerns regarding the studyDispensed study medication in a professional and accountable manner following protocol requirementsCollected, processed, and shipped blood/urine specimens at scheduled patient visitsPerformed ECGs and obtain vital signs of patientsScheduled all patient research visits and procedures consistent with protocol requirementsAdministered questionnaires/diaries per protocolEnsured that non-serious and serious adverse events are properly documented and reportedEnsured all laboratory results were given to appropriate doctors for review of clinical significance, then filed results in the patient study binderResponded to all data queries in a timely manner.Set up for monitoring visits prior to monitor’s arrival

FDA Regulations 21 CFR parts 11, 50, 54,56Informed consent processData Management System, Electronic Data Capture (EDC)GDP following ALCOA-C principlesQuality Assurance, Monitoring and Query Resolution Identification and reporting of AEs and SAEs Comprehension and execution of Clinical Trial ProtocolsMaintaining regulatory binder, housing essential documents including but not limited to 1572, Source documents, DOA, Training Logs, SAE forms, Subject Enrollment and Identification Logs, Case Report Forms (CRF), Procedure manuals, Standard Operating Procedures (SOP), Site Visit Logs, Correspondence, Trial Master Files and other Investigator site File (ISF) documents

Pasadena, California, United States

Supported Coordinators in preparing for upcoming visits including scheduling and document creation.Responded to all data queries in a timely manner.Performed a variety of tests including laboratory/phlebotomy, vital signs, ECGs, as well as other needs as outlined in the study protocol(s).Obtained medical records.Responds to patient inquires via phone or in person in a timely manner.Processed and shipped samples collected as outlined in the study protocol(s).

San Dimas, California, United States

Ramona, California, United States

Lakeside, California, United States

Bachelor Of Science - Bs, Psychology

Bachelor Of Science - Bs, Psychology, 3.0

Phlebotomy Technician/Phlebotomist