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Click here or scroll down to respond to this candidateCandidate's Name
Senior Lab DirectorPhone PHONE NUMBER AVAILABLEEMAIL AVAILABLEResearch TrainingIATA training Mayo medical LaboratoriesGCP Training CITI ProgramOHRP Office for Human Research ProtectionAdditional TrainingKUCC Customer Service Training- Team members learn how to provide exceptional care to oncology patients and their family.Jayhawk Way TrainingKUMC's success depends on having an energized and engaged workforce and a strong and compelling organizational culture. The Jayhawk Way is designed to develop leadership skills and enhance personal effectiveness.Speaker for KU Cancer Center Seminar Series regarding Clinical Pharmacology (May 2018 & May 2021) Speaker for KU Cancer Center NCI Site Visit (Feb 2012 & Feb 2022) Speaker for KUCC Annual Research Symposium (Nov 2022) Committee MemberExecutive Resource Committee, Timeline Deep Dive Committee, Deviation Resource Committee Current PositionUniversity of Kansas Cancer Center May 2022- Present Senior Lab DirectorPlan, direct, and coordinate activities in support of University of Kansas Cancer Center clinical trials regarding collection, processing, storage and transfer of tissue, blood, and excreta necessary to characterize the pharmacokinetics and pharmacodynamics of cancer therapeutic agents. Ensure effective communication, collaboration, cooperation, and coordination of Correlative Lab activities with principal investigators, study staff, the Clinical Trial Office, Clinical Pharmacology Shared Resource, and KU Health System (KUHS) associates. Responsible for providing highest quality support for clinical trials conducted at regional University of Kansas Medical Center and KUCC facilities including the Clinical Research Center, Westwood, KUMC main hospital, Cambridge Tower, and Indian Creek. This position will ensure the Correlative Lab supports protocol development, preparation of laboratory manuals, building of study-specific study kits, adequate short-term storage capacity, and transfer of samples to appropriate laboratories for analyses. In addition, this position will work with KUMC and KUHS to secure necessary capital equipment and space to conduct this important work. Previous PositionsUniversity of Kansas Cancer Center June 2019-May 2022 Correlative Lab DirectorManage all day-to-day activities in Correlative labs across KUMC campuses. Responsible for coordination of oncology clinical trials specimens and supplies per protocol requirements. Perform lab duties, manage staff, direct lab activities, communicate extensively with all project personnel and with study personnel. Responsible for quality assurance and all activities related to specimen collection, specimen handling, processing and shipping, as well as patient preparation and identification. Ensure all lab equipment is calibrated, maintained, and operable across all laboratories. Oversee all lab duties including working with clinical research team members to ensure all study samples are obtained, handled, stored, documented, and shipped in a timely manner, according to IATA regulations and protocol. Provide training and provide support for Community Sites, MCA sites and sub sites. University of Kansas Cancer Center July 2018- June 2019 Associate Project DirectorConduct Program management, project management and staff management of Kansas University Early Phase program. Prepare and submit trials to internal review committees. Manage the execution and operations of early phase trials through a cross functional team of, contract specialists, budget specialists, regulatory coordinators, and pharmacy and treatment staff. Ensure the successful completion of clinical trials according to FDA and GCP Coordinate and facilitate pre-study site visits, site initiation visits, monitoring and close out visits. Communicate monitoring/audit findings and follow up on action items. Manage and assign tasks to direct reports which include Clinical Research Coordinators and Data coordinators. Manage start-up activities, enrollment and monitoring across multiple sites.University of Kansas Cancer Center March 2015 July 2018 Correlative Lab DirectorManage all day-to-day activities in Correlative labs across KUMC campuses. Responsible for coordination of oncology clinical trials specimens and supplies per protocol requirements. Perform lab duties, manage staff, direct lab activities, communicate extensively with all project personnel and with study personnel. Responsible for quality assurance and all activities related to specimen collection, specimen handling, processing and shipping, as well as patient preparation and identification. Ensure all lab equipment is calibrated, maintained, and operable across all laboratories. Oversee all lab duties including working with clinical research team members to ensure all study samples are obtained, handled, stored, documented, and shipped in a timely manner, according to IATA regulations and protocol. Provide training and provide support for Community Sites, MCA sites and sub sites. University of Kansas Cancer Center January 2012 March 2015 Senior Lab Coordinator, Correlative studiesResponsible for coordination of oncology clinical trial study specimens, radiology data and supplies per protocol requirements. This includes pharmacokinetics, pharmacogenomics and ancillary studies for Industry-Sponsored, Cooperative Group and Investigator Initiated clinical trials. Perform all lab duties including working with clinical research team members to ensure all study samples are obtained, handled, stored, documented, and shipped in a timely manner, according to IATA regulations and protocol. Aerotek Scientific January 2012 May 2012(Staffing Agency. The Position was with the University of Kansas Cancer Center) Senior Lab Coordinator, Correlative studiesResponsible for coordination of oncology clinical trial study specimens, radiology data and supplies per protocol requirements. This includes pharmacokinetics, pharmacogenomics and ancillary studies for Industry-Sponsored, Cooperative Group and Investigator Initiated clinical trials. Perform all lab duties including working with clinical research team members to ensure all study samples are obtained, handled, stored, documented, and shipped in a timely manner, according to IATA regulations and protocol. Vince and Associates Clinical Research August 2010 January 2012 Laboratory ManagerResponsible for the coordination, planning and directing of the overall operation of the laboratory activities, in accordance with SOP policies, principles and procedures. Assist with various study related procedures such as obtaining blood and urine samples, performing ECGS and vital signs on patients. Maintain study logs and records in the laboratory, set up of new studies per protocol criteria. Assist with collecting, processing and shipping research samples in a timely manner according to IATA regulations and the protocol. Vince and Associates Clinical Research October 2009 August 2010 Research AssociateAssist with various study related procedures such as obtaining blood and urine samples, performing ECGS and vital signs on patients, processing blood and urine specimens, assisting the front office with answering inbound phone calls and filing paperwork. Assist with collecting, processing and shipping research samples to Central Laboratories according to protocol requirements.Quintiles April 2007 November 2009Clinical Enrollment TechnicianAssist with various enrollment procedures such as obtaining blood and urine specimens, obtaining ECGS and vital signs on the patients, and performing study related test on patients such as breathalyzer test, spirometry, etc. Also maintained study related responsibilities such as attending meetings and maintaining paperwork and logs for multiple studies.Research ExperienceI have over 16 years of experience in multiple therapeutic areas including oncology. I have extensive experience in management as well as experience with phlebotomy, processing, and in-house laboratory testing. I am well versed with maintaining and operating lab equipment as well as updating and maintaining laboratory records and documents per institutional guidelines. I have a background with specimen handling, processing, and shipping various specimens including pharmacokinetic, pharmacodynamics, pharmacogenomics, and tissue samples. I write Guidance Documents and SOPs for the Clinical Trials Office as needed. In addition, I have prior experience training laboratory staff and hold multiple lab related certifications such as IATA and GCP that are available upon request. |
