JOB REQUIREMENTS: Position Description: Do you want to be on the frontline of research and development fighting childhood cancer? Do you want to contribute towards the progress of better treatment and prognosis for pediatric cancer patients? Join our team of researchers at the Medical College of Wisconsin where we are conducting more than 100 clinical trials to better understand childhood cancers and blood disorders and find new ways to treat them. Under the direction of the research principal investigator and manager, the Clinical Research Coordinator I works collaboratively to support hematology, oncology, bone marrow transplant, and cellular therapy clinical trials for pediatric patients. In this role you will collaborate with the research team to coordinate subject recruitment with disease-based teammates, coordinate the collection, processing, and shipment of biologic specimens, ensure compliance to study protocol guidelines, and accurately report research data. Breakthroughs in cancer treatment don\'t happen overnight. They evolve after years of research in the laboratory, then in small groups of patients, and then in larger groups of patients. Be part of that fight! Purpose Assist in the organization and conduct of clinical trials in pediatric Oncology, Bone Marrow Transplant and Hematology. Focus is on non-therapeutics, psychology, and survivorship trials. This position manages source documentation, data reporting to sponsors, and protocol compliance. This position assists in subject recruitment, audit preparation (internal & external audits), & reporting to IRB and FDA. Primary Functions Work collaboratively to support clinical trials available to the division from consortia and cooperative groups as well as industry sponsors and investigator-initiated trials Ensure compliance with sponsoring organizations\' guidelines, as well as with relevant policies and procedures from FDA, IRB, Children\'s Wisconsin, & Medical College of Wisconsin. Coordinate subject recruitment with disease-based teammates, including: providing clinical team members with appropriate documents for obtaining informed consent, assist in obtaining informed consent, determining tests and procedures required to determine subject eligibility, and submitting necessary documentation to lead protocol organization to enroll eligible subjects. Work collaboratively with disease-based teammates to assess, track, and report adverse events, including serious adverse events, in keeping with protocol requirements. Report research data accurately and in timeframes called for by protocol. Resolve any data queires that are posed by the sponsor or... For full info follow application link. EEO/AA Minorities/Females/Vets/Disability The Medical College of Wisconsin is an affirmative action/equal opportunity employer and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, veteran status, disability or sexual orientation. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/ACEC696E1F884C34 Qualified females, minorities, and special disabled veterans and other veterans are encouraged to apply.