NYU Langone Health
Associate Clinical Research Coordinator
NYU Langone Health, New York, New York, United States, 10001
Associate Clinical Research Coordinator
NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have helped to shape the course of medical history and enrich the lives of countless people. An integral part of NYU Langone Health, the Grossman School of Medicine at its core is committed to improving the human condition through medical education, scientific research, and direct patient care. Position Summary: We have an exciting opportunity to join our team as an Associate Clinical Research Coordinator. The Non-therapeutic Oncology Associate Clinical Research Coordinator (NT aCRC) is an active participant in the coordination of oncology clinical research studies from research planning and throughout the conduct of clinical studies on various existing and upcoming protocols. The NT aCRC performs study coordination tasks under the direction of the principal investigator/treating investigator, under the supervision of CTO management/leadership and works closely with CTO staff, PCC staff, and other service rendering departments to ensure patient safety, overall compliance in the conduct of the study, adherence to the approved study protocol and quality clinical trial biospecimen and data collection. The NT aCRC interfaces directly with the Principal Investigators, various departments, research teams, and sponsors in support of the clinical trials as applicable. Job Responsibilities: - Participates in recruitment and pre-screening activities to identify diverse patients who may be eligible for clinical trials. - Collaborates with investigators, CTO staff and NYU/PCC staff to ensure a safe, compliant screening process. - Supports and conducts the informed consent process, if delegated, with the subject under the direct supervision of the PI/treating investigator. - Follows relevant institutional and departmental policies and standard operating procedures. - Registers/Randomizes subjects according to protocol. - Demonstrates understanding of protocol elements and requirements. - Provides updates to study team members regarding changes to workflow or patient-related needs. - Communicates effectively with patients. - Schedules study participants. - Prepares for upcoming study visits. - Acts as a primary point of contact for all bio-specimen collections. - Collects patient information for research projects. - Gathers and compiles data and assists in consolidating/analyzing data. - Competency in utilizing CRMS and Research Navigator. - Schedules monitoring visits. - Maintains a working knowledge of active and pipeline clinical trials. - Understands and coordinates the submission of adverse events. - Maintains trackers to ensure patients remain compliant. - May perform EKGs with documented training. - Performs concomitant medication review. - Conducts a protocol feasibility assessment. - Attends DMG and CTO meetings. - Demonstrates competence in Good Clinical Practice guidelines. - Responsible for quality source documentation. - Demonstrates self-auditing of own work. - Supports internal and external audits. - May write research notes in EPIC. Minimum Qualifications: To qualify you must have a Bachelor's Degree or equivalent combination of education and experience required. Computer literate with good interpersonal, writing and verbal communication skills. 1 years relevant experience required. Effective oral, written, communication, interpersonal skills. Must be able to work under the direction of supervision Ability to identify, analyze and solve problems. Time management skills and ability to work well under pressure. Proficiency in using various Microsoft Office applications such as Word, Excel, Access, PowerPoint and Outlook. Familiar with Internet applications. Preferred Qualifications: Bachelor's degree, preferably in science, public health, health education or a related field. Experience in oncology setting preferred. Professional certification (ACRP CCRC or SOCRA CCRP). Individuals without this certification will be encouraged to obtain this certification within one year of starting in the CRC role. 2 years experience in research or related experience preferred.
NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have helped to shape the course of medical history and enrich the lives of countless people. An integral part of NYU Langone Health, the Grossman School of Medicine at its core is committed to improving the human condition through medical education, scientific research, and direct patient care. Position Summary: We have an exciting opportunity to join our team as an Associate Clinical Research Coordinator. The Non-therapeutic Oncology Associate Clinical Research Coordinator (NT aCRC) is an active participant in the coordination of oncology clinical research studies from research planning and throughout the conduct of clinical studies on various existing and upcoming protocols. The NT aCRC performs study coordination tasks under the direction of the principal investigator/treating investigator, under the supervision of CTO management/leadership and works closely with CTO staff, PCC staff, and other service rendering departments to ensure patient safety, overall compliance in the conduct of the study, adherence to the approved study protocol and quality clinical trial biospecimen and data collection. The NT aCRC interfaces directly with the Principal Investigators, various departments, research teams, and sponsors in support of the clinical trials as applicable. Job Responsibilities: - Participates in recruitment and pre-screening activities to identify diverse patients who may be eligible for clinical trials. - Collaborates with investigators, CTO staff and NYU/PCC staff to ensure a safe, compliant screening process. - Supports and conducts the informed consent process, if delegated, with the subject under the direct supervision of the PI/treating investigator. - Follows relevant institutional and departmental policies and standard operating procedures. - Registers/Randomizes subjects according to protocol. - Demonstrates understanding of protocol elements and requirements. - Provides updates to study team members regarding changes to workflow or patient-related needs. - Communicates effectively with patients. - Schedules study participants. - Prepares for upcoming study visits. - Acts as a primary point of contact for all bio-specimen collections. - Collects patient information for research projects. - Gathers and compiles data and assists in consolidating/analyzing data. - Competency in utilizing CRMS and Research Navigator. - Schedules monitoring visits. - Maintains a working knowledge of active and pipeline clinical trials. - Understands and coordinates the submission of adverse events. - Maintains trackers to ensure patients remain compliant. - May perform EKGs with documented training. - Performs concomitant medication review. - Conducts a protocol feasibility assessment. - Attends DMG and CTO meetings. - Demonstrates competence in Good Clinical Practice guidelines. - Responsible for quality source documentation. - Demonstrates self-auditing of own work. - Supports internal and external audits. - May write research notes in EPIC. Minimum Qualifications: To qualify you must have a Bachelor's Degree or equivalent combination of education and experience required. Computer literate with good interpersonal, writing and verbal communication skills. 1 years relevant experience required. Effective oral, written, communication, interpersonal skills. Must be able to work under the direction of supervision Ability to identify, analyze and solve problems. Time management skills and ability to work well under pressure. Proficiency in using various Microsoft Office applications such as Word, Excel, Access, PowerPoint and Outlook. Familiar with Internet applications. Preferred Qualifications: Bachelor's degree, preferably in science, public health, health education or a related field. Experience in oncology setting preferred. Professional certification (ACRP CCRC or SOCRA CCRP). Individuals without this certification will be encouraged to obtain this certification within one year of starting in the CRC role. 2 years experience in research or related experience preferred.