Research - Laboratory/Non-Laboratory, Staff/Administrative
The Research Program Coordinator will be responsible for coordinating clinical research activities, including data management, maintaining IRB documents and carrying out day to day activities of clinical research projects at the Johns Hopkins University Greenberg Center for Skeletal Dysplasia. This will include pharmaceutical sponsored research and investigator-initiated research. Responsible for monitoring progress of research protocols and collection of research data on patients entered into research protocols.
Specific Duties & Responsibilities:
Will work closely with the Principal Investigator to ensure smooth and efficient execution of research protocols.
Will help coordinate patient's research visits (i.e. meeting and transporting patients), and consent research participants, collect and record research data, control data quality and maintain research integrity.
Responsible for the organization, entry, maintenance, and accuracy of all patient clinical research data in a timely and ongoing manner.
Preparing necessary paperwork packets for study visits.
Performing record reviews, using the EPIC system, and uploading the relevant materials into the online study databases.
Preparing new IRB protocols, annual renewal requests, and amendments with clinical input according to IRB for submission by the PI.
Completing and maintaining the appropriate HIPAA and Human Subjects Certifications.
Administering questionnaires to study participants.
Coordinating with the study staff of related clinical studies.
Reporting to the Principal Investigator weekly for updated list of tasks.
Recruit study participants from a clinical setting.
Performing the informed consent process with potential study participants.
Data entry into standardized computer programs including specially designed web-based programs as well as EXCEL and ACCESS databases.
Maintains good working knowledge of all assigned protocols, maintains regulatory binder for each assigned protocol, verifies patient eligibility for studies, and meets regularly with principal investigators and supervisor of studies for review data accuracy and overall progress.
The Research Program Coordinator will help in coordinating serious adverse event reporting with clinicians and investigators to insure prompt reporting to JHM IRBs and study sponsor.
Will complete all required JHMIRB submissions including annual renewals, informed consent changes, and protocol amendments. Other clinical research activities as needed.
Bachelor's degree in related discipline with some related experience required. Additional education may substitute for required experience and additional related experience may substitute for required education, to the extent permitted by the JHU equivalency formula.
JHU Equivalency Formula: 30 undergraduate degree credits (semester hours) or 18 graduate degree credits may substitute for one year of experience. Additional related experience may substitute for required education on the same basis. For jobs where equivalency is permitted, up to two years of non-related college course work may be applied towards the total minimum education/experience required for the respective job.
Classified Title: Research Program Coordinator Role/Level/Range: ACRO/03/CD Salary: $16.09 - $22.12 Status: Full-Time Work Schedule/Hours: Monday - Friday / 8:30am - 5pm Department name: 10002889-SOM Genetics Greenberg Ctr Skel Dysplasi Location: 600 N. Wolfe Street Personnel area: School of Medicine
The successful candidate(s) for this position will be subject to a pre-employment background check.
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