Clinical Research Coordinator (Radiation Oncology and Molecular Radiation S at Johns Hopkins University

Washington, District of Columbia, United States -

Full Time

Start Date

Immediate

Expiry Date

21 Aug, 26

Salary

30.3

Posted On

23 May, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trial Management, Regulatory Compliance, Data Collection, Patient Recruitment, IRB Submissions, Neurocognitive Assessment, REDCap, OnCore, Stata, Python, Medical Terminology, Project Coordination, Data Management, Interpersonal Skills, Oral and Written Communications, Attention to Detail

Industry

Education Administration Programs

Description

Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. We are seeking a Clinical Research Coordinator who will administratively coordinate clinical protocol implementation, typically for a single study. Will ensure efficient logistical implementation of the study activities and provide administrative support for research-related regulatory issues. The Clinical Research Coordinator will monitor the clinical course and collection of research data on patients participating in clinical trials at the Johns Hopkins University-Sibley Hospital location, Department of Radiation Oncology. The Clinical Research Coordinator will manage patient clinical research data which will be used to generate specific study findings. Specific Duties & Responsibilities Coordinate all activities of a clinical research study to ensure adherence to protocol and validity of findings. Participate in clinical study start-up meetings. Assist research nurses, study coordinators, principal investigators, and other study personnel in executing protocol-related activities. Explain the study background and rationale for the research to potential and current participants Contribute to the development of recruitment strategies for participants for assigned study. Implement a variety of techniques for recruitment as appropriate, e.g., print and web-based advertisements, contact referring physicians, participate in community events, etc. Independently conduct the consenting process or ensure consent is obtained on appropriate participants. Schedule participants for required activities and provide any special instructions prior to upcoming tests/exams. Serve as liaison to study participants. Assist with setup of the data collection system and enter and organize data. Assist in coordinating study meetings. Participate in study meetings and provide updates on protocol implementation status and make recommendations on operational issues. Assist with the preparation of submissions to the Institutional Review Board (IRB) Liaison with IRB on administrative matters and facilitate communications with the PI. Conduct literature searches to provide background information. Obtain and maintain excellent operating knowledge of assigned clinical protocol, clinical equipment, and clinical computer systems. Oversee budget expenditures for study operations. Other duties as assigned. In addition to the duties described above Conduct neurocognitive assessments using the following tests: California Verbal Learning Test (CVLT), NIH Toolbox, NEPSY-II/DKEFS, and Wechsler Intelligence Scale (WPPSI-IV, WISC-V, and WAIS-IV) following training Adhere to guidelines regarding honest reporting of sensitive and confidential patient information. Engage in regular contact with physicians, other health care personnel and occasionally, patients. Minimum Qualifications Bachelor's Degree in a related field. 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. Preferred Qualifications Proficient in using REDCap and/or OnCore databases. Ability to use statistical software such as Stata and experience with coding in Python. Knowledge of medical terminology. Technical Skills & Expected Level of Proficiency Attention to Detail - Awareness Clinical Trial Management System - Awareness Data Entry - Awareness Data Collection and Reporting - Awareness Data Management and Analysis - Awareness Interpersonal Skills - Awareness Oral and Written Communications - Awareness Organizational Skills - Awareness Project Coordination - Awareness Regulatory Compliance - Awareness Classified Title: Clinical Research Coordinator Role/Level/Range: ACRO37.5/03/CD Starting Salary Range: $17.20 - $30.30 HRLY ($45,000 targeted; Commensurate w/exp.) Employee group: Full Time Schedule: M-F, 8:30am-5:00pm FLSA Status: Non-Exempt Location: District of Columbia Department name: SOM Rad Onc Clinical Trials Group Personnel area: School of Medicine

Responsibilities

The coordinator will administratively manage clinical protocol implementation and monitor research data collection for patients in Radiation Oncology. Key duties include recruiting participants, conducting consenting processes, and preparing IRB submissions.