Brandon T. Email & Phone Number

Los Angeles, Ca, Us

Los Angeles, California, United States

Contract with AYA HealthcareQuality Assurance Auditing/In-House CRA

Toluca Lake, California

Contract with ActalentStudy Coordinator, working closely with study team members under the moderate direction of a Study Director, will have overall responsibilities for coordinating efforts with other study team members in order to achieve study objectives and corporate goals, including:- This will be for a high enrolling study (seeing up to 5 patients a day)- Develop strong working relationships and maintain effective communication with study team members.- Track key study metrics using tracking tools (creating and maintaining documents, tables, databases, spreadsheets and files), providing timely and quality updates to client management.- Adhere to an IRB approved protocol.- Coordinate protocol related research procedures, study visits, and follow-care.- Maintain study source documents. Report adverse events.- Educate subjects and family on protocol, study intervention, study drug, etc.- Facilitate pre-study, site qualification, study initiation, monitoring visits, and study close out activities.- Collect, process and ship laboratory specimens.- Work directly with prospective and enrolled subjects and their families or caregivers, as applicable.- May promote, advertise, and conduct telephone and face-to-shy; face screenings to recruit potential subjects.Study coordinator will work independently on site as THE research staff for Client customers.- Coordinator will be responsible for driving the success of the research studies and protocols must have a strong understanding of clinical trails and the process.- Candidate will be out on an island by themselves working directly with Sites that have not done research in the past.- Client provides the research infrastructure to physician groups and practices that want to do research and have the access to patient populations for sponsor studies

Beverly Hills, California

Contract with Insight Global - WCG ThreewireCedars-Sinai Heart Institute - Dr. Raj MakkarResearch in the Division of Interventional Cardiology- Provides general administrative support to Clinical Operations teams in completion of all required tasks to meet Sponsor goals.- Organizes, maintains, and prepares, clinical study documentation for internal/external audits, final reconciliation and archival.- Assists in quality control audits of clinical study documentation (e.g. Trial Master Files,CRF Files, Monitoring Files, etc.).- Attends project team and sponsor meetings- Collaborates with sponsors, monitors and investigators to carry out efficient and fully compliant research trials.- Adheres to standards in areas involving data collection, research protocols and regulatory reporting.- Keeps patient care protocols and clinical trial operations in compliance.- Coordinated referral physician networking, community outreach, prescreening, patient education, scheduling and administrative tasks resulting in an overall increase in patient enrollment and retention- Obtained informed consent of research subjects or guardians- Conducted informed consent presentations and maintained documentation.- Assessed records of each patient, reviewed databases and checked referrals to locate potential research study participants.- Collected, processed and delivered specimens from trial participants.- Demonstrated leadership by making improvements to work processes and helping to train others.Reason for leave: Contract assignment completed

Los Angeles, California

Contract with Actalent Kaiser Permanente LAMC - Dr. William TownerResearch in the Divisions of Infectious Disease and Vaccine- Volunteer Manager- Provides instruction to participants to teach them how to perform specific study protocols.- Prepares computer-generated reports, including statistical tables.- Answers participants' and providers' questions.- Screens and recruits’ participants; obtains consent.- Schedules examination appointments for study participants.- Conducts telephone or in-person interviews with study participants and providers.- Reviews questionnaires for completeness and accuracy; checks for inconsistencies; and codes open-ended questions. Assists with all aspects of mailed surveys.- Monitors participants' progress (e.g., blood pressure, exercise, response to questionnaires, tracking, etc.).- Provides basic data management using database software.- Maintains all pertinent project records and files.- Transcribes data from records to forms.Reason for leave: Contract assignment completed

Northridge, Ca

Research in the Divisions of Nephrology, Cardiology, and Pulmonology.Experience conducting clinical trials (Phase II - IV) and was responsible for implementing a multitude of research activities for multiple studies which includes:- Close collaboration with the Principal Investigator (PI) of each study to facilitate timely study progress reporting to the PI and enabling appropriate PI oversight, study management- Development of source worksheets/documents and safe and accurate completion of protocol required procedures in accordance with standard operating procedures, governing regulations, and study documents- Submission of eCRF documents as needed via EDC Submission (experience with imedidata, preclarus (PPD), clintrak (Medpace) and other platforms- Patient Management: recruitment, informed consent, patient interfacing, enrollment, and scheduling as well as regulatory management (IRB submissions, experience with Advarra IRB, local and central IRB)- Collecting and processing study assessments and labs such as blood draws, urine samples, ECGs, PFTand other assessments as required by study protocol- Communicating with participants regarding study objectives- Administering questionnaires and monitoring participants to ensure they adhere to compliance expectations- Liaising with laboratories regarding research findings- Monitoring the study to ensure that it complies with protocols, is ethically conducted, and follows regulatory and GCP standards- Maintaining research records of study activity, including case report forms, IP accountability and drug dispensation records or other regulatory forms as per FDA guidelines- Directing the collection, labeling, storage, and transport of all specimens whilst acting as Liaison with local and central laboratories regarding research findings- Making sure that all equipment and supplies are in-stock and in working orderReason for leave: Seeking a more established medical infrastructure vs start-up environment.

Northridge, Ca

- Provided overall specimen sample processing/shipping/liaising with local and central laboratories whilst adhering to numerous protocol schedules of operation. In addition, transporting local STAT/Routine specimen samples to local labs. - Maintaining and operating many sponsor-provided lab. equipment such as a centrifuge, refrigerated centrifuge, PCR, Incubator, etc., prepared and organized varying clinical study kits, performed experimental procedures, recorded, and consolidated research data, and executed planned research activities using observation, measurement, and analytical techniques.- Processed/Prepped/Shipped specimen samples for 15+ clinical studies. Familiarizing and corresponding with multiple sponsors that included Covance (now LabCorp), IQVIA, Syneos Health, Parexel, PPD, ICON, MedPace, Alexion, ACM, Bioclinica, Medidata, Quest Diagnostics, Signant Health, Syneos Health, etc.Reason for leave: Internship completed.

Bachelor’S, Science Of Public Health, (Bsph Program)

April 2023 (BSPH Program Resume) ONLINE August 2018 - March 2020 (BSN/RN Program Intermission due to pandemic)

High School Diploma