Teredesai, McCann & Assoc
Clinical Research Coordinator (Urology)
Teredesai, McCann & Assoc, Baltimore, Maryland, United States, 21276
Overview
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 the efficient logistical implementation of the study activities and provide administrative support for research-related regulatory issues. Responsibilities
Coordinate all activities of a clinical research study to ensure adherence to protocol and validity of findings. Participate in clinical study start-up meeting. 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 strategy 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, perform biospecimen collection, including blood draws and other sample types, following IRB-approved protocols and ensuring proper labeling and documentation. Process, aliquot, and store biological samples according to study-specific and biorepository SOPs to maintain specimen integrity and compliance with quality standards. 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
Related undergraduate or work experience in human subject's research. 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. Additional Information
Classified Title: Research Project Coordinator Job Posting Title (Working Title): Clinical Research Coordinator (Urology) Role/Level/Range: ACRO40/E/03/CD Starting Salary Range: $17.20 - $30.30 HRLY ($49,400 targeted; Commensurate w/exp.) Employee group: Full Time Schedule: Monday - Friday, 8:30am - 5:00pm FLSA Status: Non-Exempt Location: School of Medicine Campus Department name: SOM Uro Urology Research Personnel area: School of Medicine Salary and benefits information, equity statements, and equal opportunity notices follow Johns Hopkins University policies. The university is an Equal Opportunity Employer and does not discriminate on the basis of sex, gender, marital status, pregnancy, race, color, ethnicity, national origin, age, disability, religion, sexual orientation, gender identity or expression, veteran status or other legally protected characteristic. EEO is the Law: 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. Accommodation Information: If you require special assistance or accommodation during any part of the pre-employment process, please contact the Talent Acquisition Office.
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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 the efficient logistical implementation of the study activities and provide administrative support for research-related regulatory issues. Responsibilities
Coordinate all activities of a clinical research study to ensure adherence to protocol and validity of findings. Participate in clinical study start-up meeting. 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 strategy 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, perform biospecimen collection, including blood draws and other sample types, following IRB-approved protocols and ensuring proper labeling and documentation. Process, aliquot, and store biological samples according to study-specific and biorepository SOPs to maintain specimen integrity and compliance with quality standards. 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
Related undergraduate or work experience in human subject's research. 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. Additional Information
Classified Title: Research Project Coordinator Job Posting Title (Working Title): Clinical Research Coordinator (Urology) Role/Level/Range: ACRO40/E/03/CD Starting Salary Range: $17.20 - $30.30 HRLY ($49,400 targeted; Commensurate w/exp.) Employee group: Full Time Schedule: Monday - Friday, 8:30am - 5:00pm FLSA Status: Non-Exempt Location: School of Medicine Campus Department name: SOM Uro Urology Research Personnel area: School of Medicine Salary and benefits information, equity statements, and equal opportunity notices follow Johns Hopkins University policies. The university is an Equal Opportunity Employer and does not discriminate on the basis of sex, gender, marital status, pregnancy, race, color, ethnicity, national origin, age, disability, religion, sexual orientation, gender identity or expression, veteran status or other legally protected characteristic. EEO is the Law: 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. Accommodation Information: If you require special assistance or accommodation during any part of the pre-employment process, please contact the Talent Acquisition Office.
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