NYU Langone Health
Associate Clinical Research - Fulltime - Monday - Friday - 9 am - 5 pm
NYU Langone Health, New York, New York, us, 10261
Associate Clinical Research - Fulltime - Monday - Friday - 9 am - 5 pm
Associate Clinical Research - Fulltime - Monday - Friday - 9 am - 5 pm role at
NYU Langone Health NYU Langone Hospital—Brooklyn is a full-service teaching hospital and Level I trauma center located in Sunset Park, Brooklyn. The hospital is central to a comprehensive network of affiliated ambulatory and outpatient practices, and serves as NYU Langone Health's anchor for healthcare access, growth, and delivery in the entire borough. At NYU Langone Health, equity and inclusion are fundamental values. We strive to be a place where our exceptionally talented faculty, staff, and students of all identities can thrive. Position Summary We have an exciting opportunity to join our team as a Associate Clinical Research - Fulltime - Monday - Friday - 9 am - 5 pm.
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. 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 to ensure safe, compliant and quality research conduct. Registers/Randomizes subjects according to protocol and internal CTO policies. Demonstrates understanding of protocol elements and requirements. Provides updates to study team members regarding changes to workflow or patient-related needs according to protocol modifications. Communicates effectively with patients and assists them in understanding/navigating non-clinical study related concerns. Schedules study participants according to the approved protocol. Prepares for upcoming study visits: research bio-specimen collection order preparation/placement, laboratory and EKG order placement. Acts as a primary point of contact for all bio-specimen collections. Collects patient information for research project. Gathers and compiles data and assists in consolidating/analyzing data for presentation to sponsoring and regulatory agencies. Competency in utilizing CRMS and Research Navigator for day-to-day tasks. Schedules monitoring visits as needed. Maintains a working knowledge of active and pipeline clinical trials within the DMG. Understands and coordinates the submission of adverse events per protocol and per institutional and FDA guidelines. Maintains trackers to ensure patients remain compliant with study specific requirements and tasks. Compiles and submits weekly patient lists to RBMU and other departments as needed. May perform EKGs with documented training. Performs concomitant medication review including reconciliation of the medication list. Maintain a clear, clean follow up calendar for the CCU DMG team. Conducts a protocol feasibility assessment per institutional guidelines. Attends DMG and CTO meetings to support patient care, quality research conduct. Demonstrates competence in Good Clinical Practice (GCP) guidelines, Federal Regulations that govern and conduct human subject’s research. Responsible for quality source documentation following ALCOA-C standards. Protects patient confidentiality and PHI and complies with HIPAA. Demonstrates self-auditing of own work to ensure protocol compliance and patient safety. Utilizes principles of HRO in day-today-work and communication to ensure safe, quality clinical research conduct. Supports internal audits and preparation for external audits as needed across the CTO. May write research notes in EPIC to support clear clinical trial documentation. Performs other duties as assigned and additional responsibilities as needed. Minimum Qualifications To qualify you must have a Associate Degree, Computer literate with good interpersonal, writing and verbal communication skills, and 1-year experience in a healthcare related position required. Knowledge, Skills And Abilities Proficiency in using various Microsoft Office applications, Intermediate competency in medical terminology, and Good Clinical Practice (GCP) guidelines. Preferred Qualifications Bachelors degree, preferably in science, public health, health education or a related field, Professional certification (ACRP CCRC or SOCRA CCRP), and 1-2 Years Experience In Research Or Related Experience Preferred.
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Associate Clinical Research - Fulltime - Monday - Friday - 9 am - 5 pm role at
NYU Langone Health NYU Langone Hospital—Brooklyn is a full-service teaching hospital and Level I trauma center located in Sunset Park, Brooklyn. The hospital is central to a comprehensive network of affiliated ambulatory and outpatient practices, and serves as NYU Langone Health's anchor for healthcare access, growth, and delivery in the entire borough. At NYU Langone Health, equity and inclusion are fundamental values. We strive to be a place where our exceptionally talented faculty, staff, and students of all identities can thrive. Position Summary We have an exciting opportunity to join our team as a Associate Clinical Research - Fulltime - Monday - Friday - 9 am - 5 pm.
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. 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 to ensure safe, compliant and quality research conduct. Registers/Randomizes subjects according to protocol and internal CTO policies. Demonstrates understanding of protocol elements and requirements. Provides updates to study team members regarding changes to workflow or patient-related needs according to protocol modifications. Communicates effectively with patients and assists them in understanding/navigating non-clinical study related concerns. Schedules study participants according to the approved protocol. Prepares for upcoming study visits: research bio-specimen collection order preparation/placement, laboratory and EKG order placement. Acts as a primary point of contact for all bio-specimen collections. Collects patient information for research project. Gathers and compiles data and assists in consolidating/analyzing data for presentation to sponsoring and regulatory agencies. Competency in utilizing CRMS and Research Navigator for day-to-day tasks. Schedules monitoring visits as needed. Maintains a working knowledge of active and pipeline clinical trials within the DMG. Understands and coordinates the submission of adverse events per protocol and per institutional and FDA guidelines. Maintains trackers to ensure patients remain compliant with study specific requirements and tasks. Compiles and submits weekly patient lists to RBMU and other departments as needed. May perform EKGs with documented training. Performs concomitant medication review including reconciliation of the medication list. Maintain a clear, clean follow up calendar for the CCU DMG team. Conducts a protocol feasibility assessment per institutional guidelines. Attends DMG and CTO meetings to support patient care, quality research conduct. Demonstrates competence in Good Clinical Practice (GCP) guidelines, Federal Regulations that govern and conduct human subject’s research. Responsible for quality source documentation following ALCOA-C standards. Protects patient confidentiality and PHI and complies with HIPAA. Demonstrates self-auditing of own work to ensure protocol compliance and patient safety. Utilizes principles of HRO in day-today-work and communication to ensure safe, quality clinical research conduct. Supports internal audits and preparation for external audits as needed across the CTO. May write research notes in EPIC to support clear clinical trial documentation. Performs other duties as assigned and additional responsibilities as needed. Minimum Qualifications To qualify you must have a Associate Degree, Computer literate with good interpersonal, writing and verbal communication skills, and 1-year experience in a healthcare related position required. Knowledge, Skills And Abilities Proficiency in using various Microsoft Office applications, Intermediate competency in medical terminology, and Good Clinical Practice (GCP) guidelines. Preferred Qualifications Bachelors degree, preferably in science, public health, health education or a related field, Professional certification (ACRP CCRC or SOCRA CCRP), and 1-2 Years Experience In Research Or Related Experience Preferred.
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