San Diego Metropolitan Area
Oncology
•Responsible for coordinating and managing clinical trial activity conducted at the UCSD Hillcrest location •Serve as a liaison and establishes standard operating procedures across departments for the purpose of implementation of studies •Provide all aspects of protocol management such as screening for patient eligibility, data collection and analysis, ensuring protocol compliance, adverse drug reaction reporting, monitoring patient treatment and toxicities, laboratory and specimen submissions, and maintenance of accurate and complete clinical research files for all oncology studies •Led corrective and preventative action (CAPA) plan to ensure ongoing regulatory compliance of NCI protocols
Head and Neck Oncology Clinical Trial Coordination •Adhere to Federal, State, and Institutional polices to ensure completion of clinical trials according to FDA, GCP, and Human Research Protections Program approvals and regulations •Independently utilize clinical knowledge and institutional policies to coordinate clinical trial subjects’ screening, enrollment, randomization and scheduling in accordance with large complex, multi-center clinical research protocols •Serve as a primary coordinating line of communication among clinic, laboratory, pharmacy, Clinical Research Organizations, and clinical trial sponsor personnel for the implementation, operation, and query resolution for clinical trials •Provide education and information to potential trial subjects regarding the following: trial procedures, medications, risks, cost-compensation, or other trial related information •Develop clinical trial source documentation to monitor subjects’ protocol adherence, treatment outcomes, and medical record to ensure accurate and timely data reporting •Obtain and process, store and/ or ship human biological samples •Contribute to development, and improvement of clinical trial workflows, and logistics management by providing disease team leadership feedback Training •Develop and maintain Clinical Research Coordinator training, data source templates, eCRFs, start-up requirements, and other resources for clinical research staff •Serve as primary contact for clinical research staff for training, operational guidance, and troubleshooting •Provide leadership to new hires and other support personnel Clinical Trials Provide preparation and compliance support during clinical trial start up •Provide biospecimen collection support to include trial supplies ordering, sample processing and shipping, and sub-site kit assembly •Monitor trial subject binders for CRF/eCRF completion, data accuracy and query resolution •Initiate, manage, and maintain complex NIH multisite study
Interventional and Nuclear Cardiology • Back office duties such an obtaining vitals, performing EKGs, and various blood work • Assessing patients for initial symptoms and patient history • Scribing details of visit and assembling treatment plan • Manage hospital and clinic schedule for the physicians of the practice
• Patient floor aid in women’s center, MICU, SICU, transition care unit • Pharmacy runner- deliver patient medications to designated parts of the hospital • Volunteer office clerk and Main Lobby Clerk
• Tutor students in math and science • Conduct evidence based tutorials • Grading student papers and assisting teachers