Research Services Coordinator

Develops and implements materials for communications with partners and participating practices, including generating and updating website content, developing newsletters and presentations, and managing email listservs. Communicates and builds connections with external partners, including agencies of the State of Colorado, practice transformation organizations (PTOs), various other community organizations, primary care practices, external funders, and other academic departments and institutions. Works with project teams to set agendas, develop processes, manage needed follow-up activities, and ensure consistent support necessary to sustain the successful implementation of Practice Innovation Projects.

Research Services Professional

Assist with and oversee the day-to-day operations of clinical trials and studies. Obtain study subject’s social network data and current tobacco use information, review research protocol inclusion/exclusion criteria, and confirm eligibility of subject to participate in clinical trial. Perform informed consent process or ensures that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required. Interview prospective subjects for a variety of research clinical trials. Educates potential subjects on the details of the studies through phone contacts and personal interviews. Schedule subject participation in research clinical trial, coordinating subject access to web-based study resources, completion of online and text-based surveys, and provide basic technical support.

Research Services Senior Professional

Assist with and oversee the day to day operations of clinical trials and studies. Collect, code, and analyze data obtained from research in an accurate and timely manner. Adhere to research regulatory standards. Maintain detailed records of studies to ensure compliance with requirements of the Food and Drug Administration (FDA), study protocols, department, hospital/clinical standard operating procedures and other regulatory guidelines.Assist with developing or develops protocol-specific systems and documents including process flows, training manuals, Standard Operating Procedures (SOPs) and Case Report Forms (CRFs). Maintains subject level documentation and prepares documents, equipment and/or supplies. Assist with identifying issues related to operational efficiency and shares results with leadership

All positions require a minimum of a Bachelor's Degree in a science, social sciences, healthcare, or communication or a related field. Master's preferred. Experience in supporting research projects required.

 

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