Johns Hopkins University
Location
Baltimore, Maryland
Salary
$41,300 - $72,300 / YEAR
Oversee day-to-day activities of complex pulmonary clinical research studies and ensure operational feasibility of protocols. Manage participant recruitment, data collection systems, and maintain compliance with all applicable regulations and IRB requirements.
Requires a Bachelor's degree in a related field and at least three years of related experience. A Master's degree in a related field is preferred.
Assist Principal Investigator or more senior research staff to ensure operational feasibility of proposed protocol/study design. Develop standard operating procedures and data collection forms from protocol(s). Develop consent form(s) for clinical trials based on protocol(s). Prepare materials for submission to IRB. Contribute to work with commercial and/or government agency sponsors and recommend which group can commit to considering patient population, available resources, and cost of providing services. Ensure compliance with all protocols, procedures, and applicable regulations. Participate in developing the study budget. Develop and oversee the implementation of recruitment strategy for participants for one or more assigned studies. Set up a data collection system and ensure the validity of study data. Organize and quality control study data Perform self-audits and/or audit other sites. Participate in study meetings and provide status updates and recommend changes to protocol operations based on results and goals. Conduct literature searches to provide background information. Abstract and index information based on knowledge of subject matter. Other duties as assigned.
Bachelor's Degree in a related field. Three years of related experience. Additional education may substitute for required experience and additional related experience may substitute for required education beyond a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula.
Master's Degree in a related field. Classified Title: Sr. Clinical Research Coordinator Role/Level/Range: ACRP/03/MB Starting
$41,300 - $72,300 Annually ($60,000 targeted; Commensurate w/exp.) Employee group: Full Time Schedule: Monday to Friday 8:30 -5pm. (earlier/later on some days); occasional nights/weekends if needed for a study FLSA Status: Exempt Location: School of Medicine Campus Department name: SOM DOM Pulmonary Personnel area: School of Medicine
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