Reporting directly to the Disease Team Project Manager, the Clinical Research Coordinator I is responsible for coordinating and managing clinical trials including providing all aspects of protocol management, including screening for patient eligibility, data collection and analysis, ensuring protocol compliance, adverse drug reaction reports, monitoring patient treatment and toxicities, laboratory and specimen submission, and maintenance of accurate and complete clinical research files. Assist the regulatory department with Human subjects submissions, renewals, and safety reports. Directly communicate with assigned physicians and disease groups, including attending weekly meetings and tumor boards. Provide direct assistance to the Project Manager in reviewing and verifying university research account statements, professional fee statements, and invoicing. Other duties assigned as needed.

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Under the supervision of a Principal Investigator, the incumbent will apply a wide variety of experimental research techniques to problems of cell growth and oncogenic transformation related to gastrointestinal cancer. Collaborate with PI on methods to the investigation cell signaling and their respective roles in processes associated with tumor progression. Additionally, the incumbent will provide bioinformatics, statistical, data management and report support for computational analyses and lab research with primary analysis focus in multi-omic analyses. Perform advanced data analysis and statistical methodologies based on integrative approaches including, e.g., genomic, proteomic, clinical and other types of data. Independently perform routine laboratory experiments, such as immunoblotting, cell viability assays, confocal microscopy, Real-Time PCR analyses and immunofluorescence, cell cycle analysis of in-vitro cell lines. Independently work on data preparation for large scale data analysis and provide support for manuscript publication.

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