Research Data Coordinator Salary in Kansas

Job Type Full-time Description Hematology Oncology Associates of CNY (HOACNY), voted one of Central New York's Best Places to Work, is looking for a full time Research Data Coordinator to join our professional team. HOACNY provides cancer care services, Monday through Friday, at three convenient locations in East Syracuse, Syracuse and Auburn. If you are a highly motivated, team oriented individual looking to make a difference in your career, please apply now. Research Data Coordinator -Competitive Pay-Bonuses/Stipends as well as a generous benefits package including medical, dental, life, std, ltd, 401k/pension, tuition reimbursement, holidays, advanced PTO etc. Convenient, free parking. The Research Data Coordinator is responsible for managing and submitting data for assigned patients, checking research admits and obits daily, assisting research staff and lab with research study specimens, monitoring QA for department, screening for eligible patients and various other duties as reque

The University of Alabama at Birmingham, O'Neal Comprehensive Cancer Center, is seeking a Manager of Clinical Research Data Coordination to join our team. The Manager for Clinical Research Data Coordination will serve as the O'Neal Clinical Trial Office expert on data reporting responsibilities, various sponsor and IT data capture platforms and will lead, manage, and train new staff as well as design, implement and interpret research data projects. The O'Neal Comprehensive Cancer Center is one of 51 NCI-designated comprehensive cancer centers in the United States and is the only one in Alabama and in the Deep South region. A comprehensive designation also means UAB Medicine patients have access to leading-edge treatments or clinical trials that they may not otherwise have at local community hospitals or smaller cancer centers. For many, an NCI designation can hold the key to survival. The link to our website is https://www.uab.edu/onealcancercenter/. * Please attached a current resume

Position Summary Clinical Research Data Coordinator III (CRDC III) will conduct research study activities, with oversight from the Program Manager and Principal Investigator(s), in accordance with the protocol, IRB regulations, and Good Clinical Practice (GCP). This individual will perform procedures as required by the protocol, including design, implementation, and maintenance of clinical-based relational database management systems. The CRDC III will ensure the operation and maintenance of departmental systems for data organization, collection, retrieval, and reporting purposes. They will develop methods for tracking and reporting data and monitoring incoming and outgoing data to ensure data integrity and compliance with applicable regulatory agency policy. CRDC III will take part in the development of scientific reports and publications and will be a liaison between faculty, CRDC II, other study personnel, and data entry personnel. The CRDC III will perform statistical analyses, inc

The primary purpose of this position is to provide exceptional patient-facing research care for the Lymphoma Observational & Translational Research (LOTR) program within the Department of Lymphoma and Myeloma. The incumbent provides education to patients on research protocols and is knowledgeable about proper human subject research guidelines. Job Specific Competencies: Clinical Research Support (70%) * Perform informed consent procedures for minimal risk research protocols in accordance with institutional policies and research guidelines. * Screen for and identify patients based on protocol eligibility and exclusion criteria. * Provide patients with adequate education to consider enrollment in research studies for which they meet enrollment criteria. * Assist patients in completing study questionnaires and other study procedures. Translational Research Support (20%) * Screen for and identify standard of care biospecimen collections needed for research. * Collect and distribute researc

The primary purpose of this position is to provide exceptional patient-facing research care for the Lymphoma Observational & Translational Research (LOTR) program within the Department of Lymphoma and Myeloma. The incumbent provides education to patients on research protocols and is knowledgeable about proper human subject research guidelines. Job Specific Competencies: Clinical Research Support (70%) * Perform informed consent procedures for minimal risk research protocols in accordance with institutional policies and research guidelines. * Screen for and identify patients based on protocol eligibility and exclusion criteria. * Provide patients with adequate education to consider enrollment in research studies for which they meet enrollment criteria. * Assist patients in completing study questionnaires and other study procedures. Translational Research Support (20%) * Screen for and identify standard of care biospecimen collections needed for research. * Collect and distribute researc

Primary Purpose of Organizational Unit The UNC School of Medicine has a rich tradition of excellence and care. Our mission is to improve the health and wellbeing of North Carolinians, and others whom we serve. We accomplish this by providing leadership and excellence in the interrelated areas of patient care, education, and research. We strive to promote faculty, staff, and learner development in a diverse, respectful environment where our colleagues demonstrate professionalism, enhance learning, and create personal and professional sustainability. We optimize our partnership with the UNC Health System through close collaboration and commitment to service. OUR VISION Our vision is to be the nation's leading public school of medicine. We are ranked 2nd in primary care education among all US schools of medicine and 5th among public peers in NIH research funding. Our Allied Health Department is home to five top-ranked divisions, and we are home to 18 top-ranked clinical and basic science