Nationwide Children's Hospital
Clinical Research Coordinator II - RI Rheumatology
Nationwide Children's Hospital, Columbus, Ohio, United States, 43224
Clinical Research Coordinator II - RI Rheumatology
Requisition ID
2024-53084
Category
Research
Overview
The Clinical Research Coordinator II is responsible for managing all of the elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. These elements include but are not limited to; start-up activities, launch activities, day to day management of a study and study closure activities. The CRC II also trains and mentors other CRC's to ensure consistency in study management activities.Why Nationwide Children's Hospital?
The moment you walk through our doors, you feel it. When you meet our patient families, you believe it. And when you talk with anyone who works here, you want to be part of it. Welcome to Nationwide Children's Hospital,
Where Passion Meets Purpose
.Here,
Diversity, Equity and Inclusion
are integrated into our core values and practices. We are passionate about building, sustaining and evolving an inclusive and equitable environment. We are seeking individuals who live these values and want to share their experiences and efforts in support of our collective mission.We're 14,000 strong. And it takes every one of us to improve the lives of the kids we care for, and the kids around the world we'll never meet. Kids who live healthier, fuller lives because of the knowledge we share. We know it takes
a Collaborative Culture
to deliver on our promise to provide the very best, innovative care and to foster new discoveries, made possible by the most groundbreaking research. Anywhere.Ask anyone with a Nationwide Children's badge what they do for a living. They'll tell you it's
More Than a Job
. It's a calling. It's a chance to use and grow your talent to make an impact that truly matters. Because here, we exist simply to help children everywhere.Nationwide Children's Hospital.
A Place to Be Proud
.Responsibilities
Conducts clinical studies as outlined in the study protocol; discerns critical elements of the protocol to ensure subject safety throughout study; adheres to good clinical practices.
Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects' rights through institutional IRB, federal and state regulations; Ensures the subject meets inclusion/exclusion criteria; answers questions related to the protocol procedure as applicable; acts as a patient/family advocate;Coordinates, and schedules subject study visits with other hospital services and the PI/sub-I; manages protocol required data; performs study procedures according to recognized skill level and certifications and within the local and federal regulations and guidelines; collects, processes and ships human specimens for use in research studiesIdentifies study implementation and/or study management issues and works with the study team to develop and implement solutions to ensure study progress and successAssists with the study recruitment plan and provides input into the study budget; manages all screening, enrollment and study participation logs; completes recruitment summary at study termination.Creates source documents that facilitate systematic data collection and/or aid in protocol execution and management and record keeping; and conducts accurate and timely subject data collection,Assists with study database development to maintain study data in identified format, according to recognized skill level; completes Case Report Forms (CRF's) and ensures CRF's are completed prior to monitor visits.Educates other study personnel with regards to study-specific responsibilities and keeps written documentation of this training.Alerts the investigator when the subject's safety is in jeopardy, there is aprotocol deviation, or when the subject requests premature study termination.Responsible for regulatory/IRB issues after a study has been initiated; maintains regulatory binder.Assists the principal investigator in the preparation of scientific publications and grant proposals.
Qualifications
BA/BS preferred; Associates degree or equivalent work-related experiencerequired.CRA/CRC certification preferred.Minimum of 18 months experience in clinical research or health care field, twoyears preferred.Understanding of medical terminology and clinical trials preferred.Working knowledge of PCs and word processing and data managementsoftwareDemonstrated analytical skills with accuracy and attention to detail.Excellent verbal and written communication skills.Goal-oriented and self-directive, ability to manage complex projectsindependently.Strong organizational and interpersonal skills.Ability to actively participate as a team playerThe above list of duties is intended to describe the general nature and level of work performed by individualsassigned to this classification. It is not to be construed as an exhaustive list of duties performed by the individualso classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the workof employees under his/her supervision.EOE M/F/Disability/VetNeed help finding the right job?
We can recommend jobs specifically for you!Click here to get started.
Requisition ID
2024-53084
Category
Research
Overview
The Clinical Research Coordinator II is responsible for managing all of the elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. These elements include but are not limited to; start-up activities, launch activities, day to day management of a study and study closure activities. The CRC II also trains and mentors other CRC's to ensure consistency in study management activities.Why Nationwide Children's Hospital?
The moment you walk through our doors, you feel it. When you meet our patient families, you believe it. And when you talk with anyone who works here, you want to be part of it. Welcome to Nationwide Children's Hospital,
Where Passion Meets Purpose
.Here,
Diversity, Equity and Inclusion
are integrated into our core values and practices. We are passionate about building, sustaining and evolving an inclusive and equitable environment. We are seeking individuals who live these values and want to share their experiences and efforts in support of our collective mission.We're 14,000 strong. And it takes every one of us to improve the lives of the kids we care for, and the kids around the world we'll never meet. Kids who live healthier, fuller lives because of the knowledge we share. We know it takes
a Collaborative Culture
to deliver on our promise to provide the very best, innovative care and to foster new discoveries, made possible by the most groundbreaking research. Anywhere.Ask anyone with a Nationwide Children's badge what they do for a living. They'll tell you it's
More Than a Job
. It's a calling. It's a chance to use and grow your talent to make an impact that truly matters. Because here, we exist simply to help children everywhere.Nationwide Children's Hospital.
A Place to Be Proud
.Responsibilities
Conducts clinical studies as outlined in the study protocol; discerns critical elements of the protocol to ensure subject safety throughout study; adheres to good clinical practices.
Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects' rights through institutional IRB, federal and state regulations; Ensures the subject meets inclusion/exclusion criteria; answers questions related to the protocol procedure as applicable; acts as a patient/family advocate;Coordinates, and schedules subject study visits with other hospital services and the PI/sub-I; manages protocol required data; performs study procedures according to recognized skill level and certifications and within the local and federal regulations and guidelines; collects, processes and ships human specimens for use in research studiesIdentifies study implementation and/or study management issues and works with the study team to develop and implement solutions to ensure study progress and successAssists with the study recruitment plan and provides input into the study budget; manages all screening, enrollment and study participation logs; completes recruitment summary at study termination.Creates source documents that facilitate systematic data collection and/or aid in protocol execution and management and record keeping; and conducts accurate and timely subject data collection,Assists with study database development to maintain study data in identified format, according to recognized skill level; completes Case Report Forms (CRF's) and ensures CRF's are completed prior to monitor visits.Educates other study personnel with regards to study-specific responsibilities and keeps written documentation of this training.Alerts the investigator when the subject's safety is in jeopardy, there is aprotocol deviation, or when the subject requests premature study termination.Responsible for regulatory/IRB issues after a study has been initiated; maintains regulatory binder.Assists the principal investigator in the preparation of scientific publications and grant proposals.
Qualifications
BA/BS preferred; Associates degree or equivalent work-related experiencerequired.CRA/CRC certification preferred.Minimum of 18 months experience in clinical research or health care field, twoyears preferred.Understanding of medical terminology and clinical trials preferred.Working knowledge of PCs and word processing and data managementsoftwareDemonstrated analytical skills with accuracy and attention to detail.Excellent verbal and written communication skills.Goal-oriented and self-directive, ability to manage complex projectsindependently.Strong organizational and interpersonal skills.Ability to actively participate as a team playerThe above list of duties is intended to describe the general nature and level of work performed by individualsassigned to this classification. It is not to be construed as an exhaustive list of duties performed by the individualso classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the workof employees under his/her supervision.EOE M/F/Disability/VetNeed help finding the right job?
We can recommend jobs specifically for you!Click here to get started.