The Johns Hopkins University
Research Program Coordinator - 118025
The Johns Hopkins University, Baltimore, Maryland, United States, 21276
The Department of Neurology is seeking a
Research Program Coordinator
who will be responsible for coordinating clinical trials and other clinical research projects in the Johns Hopkins Multiple Sclerosis Center. This may involve screening medical records, identifying appropriate patients, consenting study participants, performing data collection and entry, obtaining and processing specimens (e.g., blood, urine), and organizing regulatory paperwork. Specific Duties & Responsibilities Maintain a good working knowledge of all assigned protocols and projects and their reporting requirements and will adhere to all protocol and regulatory requirements to ensure the validity of the clinical research data. Work directly with the principal investigators and other study coordinators to execute multiple study protocols. May also be involved in the amendment of existing protocols or development of new study protocols. Attend clinics, screen potential participants, and carry out research-related procedures with participants on a daily basis. Monitor, schedule, and execute participants' study visits and may be involved in reconciling study-related invoices. Manage and maintain all participant binders, study binders, and documentation for the study as well as assist the principal investigators in preparing for audits, advertising for the studies, implementing new recruitment strategies, and preparing reports for the IRB as well as handling and documenting IRB correspondence. May attend educational lectures and conferences. Must be willing to conduct database management. The position reports to the Research Nurse, with an indirect reporting line to the faculty principal investigators of the clinical research projects. Minimum Qualifications Bachelor's Degree in related discipline. Additional related experience may substitute for required education, to the extent permitted by the JHU equivalency formula. Additional education may substitute for required experience and additional related experience may substitute for required education beyond HS Diploma/Graduation Equivalent, to the extent permitted by the JHU equivalency formula. Preferred Qualifications Some experience with Stata, ACCESS, and REDCap preferred. Experience with Microsoft Word and Excel. Phlebotomy skills preferred (or willingness to learn) The Johns Hopkins University is an equal opportunity employer and welcomes applications from diverse candidates. The university is committed to hiring individuals with a justice-involved background, consistent with applicable policies and current practice. Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
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Research Program Coordinator
who will be responsible for coordinating clinical trials and other clinical research projects in the Johns Hopkins Multiple Sclerosis Center. This may involve screening medical records, identifying appropriate patients, consenting study participants, performing data collection and entry, obtaining and processing specimens (e.g., blood, urine), and organizing regulatory paperwork. Specific Duties & Responsibilities Maintain a good working knowledge of all assigned protocols and projects and their reporting requirements and will adhere to all protocol and regulatory requirements to ensure the validity of the clinical research data. Work directly with the principal investigators and other study coordinators to execute multiple study protocols. May also be involved in the amendment of existing protocols or development of new study protocols. Attend clinics, screen potential participants, and carry out research-related procedures with participants on a daily basis. Monitor, schedule, and execute participants' study visits and may be involved in reconciling study-related invoices. Manage and maintain all participant binders, study binders, and documentation for the study as well as assist the principal investigators in preparing for audits, advertising for the studies, implementing new recruitment strategies, and preparing reports for the IRB as well as handling and documenting IRB correspondence. May attend educational lectures and conferences. Must be willing to conduct database management. The position reports to the Research Nurse, with an indirect reporting line to the faculty principal investigators of the clinical research projects. Minimum Qualifications Bachelor's Degree in related discipline. Additional related experience may substitute for required education, to the extent permitted by the JHU equivalency formula. Additional education may substitute for required experience and additional related experience may substitute for required education beyond HS Diploma/Graduation Equivalent, to the extent permitted by the JHU equivalency formula. Preferred Qualifications Some experience with Stata, ACCESS, and REDCap preferred. Experience with Microsoft Word and Excel. Phlebotomy skills preferred (or willingness to learn) The Johns Hopkins University is an equal opportunity employer and welcomes applications from diverse candidates. The university is committed to hiring individuals with a justice-involved background, consistent with applicable policies and current practice. Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
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