Research Program Coordinator
About The Position
The Department of Neurology is seeking a Research Program Coordinator who will coordinate clinical trials and other clinical research projects in the Johns Hopkins Multiple Sclerosis Center. This may involve, but is not limited to screening medical records, identifying appropriate patients, consenting study participants, performing data collection and entry, obtaining and processing specimens (e.g., blood, urine), organizing regulatory paperwork, accompanying patients to and from various clinic areas. This is an on site position that will report to the Sr. Research Program Manager, with an indirect reporting line to the faculty principal investigators of the clinical research projects.
Requirements
- Must have professional attitude and excellent communication skills, including oral and written communication, as well as outstanding interpersonal skills.
- Must have a mature outlook, be self-motivated and be highly organized.
- Must be able to work independently complete tasks, work with others to problem solve, be detail-oriented, and able to multi-task.
- Experience with Microsoft Word and Excel required.
- Bachelor's Degree in related discipline.
- Additional related experience may substitute for required education, to the extent permitted by the JHU equivalency formula.
Nice To Haves
- Experience with RedCap, EPIC, IRB, and OnCore preferred.
- Phlebotomy skills preferred (or willingness to learn).
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.
- Attends clinics, screens potential participants, and carries out research-related procedures with them daily.
- 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.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Industry
Educational Services
Number of Employees
5,001-10,000 employees
