Nationwide Children's Hospital

Clinical Research Coordinator II - Child Development Center

Posted Date 7 months ago(3/11/2020 4:25 PM)
Requisition ID


Posting Title:  Clinical Research Coordinator II - Child Development Center


Date Posted:  March 11, 2020                          Fulltime | Benefit's Eligible



Ctr Autism Spectrum Disorder
187 W Schrock Rd
Westerville, Ohio 43081


We are seeking a Clinical Research Coordinator II - Child Development Center.  This position 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 can feel it. When you meet one of our patient families, you believe it. And when you talk with anyone who works here, you want to be part of it, too. Welcome to Nationwide Children’s Hospital, where Passion Meets Purpose.

Here, Everyone Matters. We’re 13,000 strong. And it takes every single one of us to improve the lives of the kids we care for, and the kids from around the world we’ll never even meet. Kids who are living 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.

What Will You Be Doing?

  • 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 studies
  • Identifies study implementation and/or study management issues and works with the study team to develop and implement solutions to ensure study progress and success
  • Develops 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,
  •  Develops study database to maintain study data in de-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 responsibilities and keeps written documentation of this training.
  •  Alerts the investigator when the subject’s safety is in jeopardy, there is a protocol 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.
  •  Trains and mentors other clinical research coordinators.
  •  Performs other duties and maintains flexible schedule as required by a protocol or unit needs.


What Are We Looking For?


To fulfill this role successfully, you must possess these minimum qualifications and experience:

  • BA/BS preferred; Associates degree or equivalent work related experience required;
  • Minimum of 2 years of experience in clinical research or health care field.
  • Understanding of medical terminology and clinical trials preferred.
  • CRA/CRC certification preferred.

Skills required:

  • Working knowledge of PCs and word processing and data management software
  • Verbal and written communication
  • Goal-oriented; self-directive
  • Initiation, motivation, creativity
  • Organizational and interpersonal
  • Ability to actively participate as a team player
  • Mentoring/training of new CRC’s

Your Benefits, Your Wellness:

As an employer, Nationwide Children’s recognizes the importance of the benefits we offer. We also recognize the importance of balancing your work and personal needs.  Our benefits and Employee Wellness package is designed to:

  • Empower you to be a conscientious health care consumer through educational and wellness activities
  • Establish a work environment that promotes health and well-being
  • Support your financial protection and security in retirement

Most of our positions are benefits’ eligible from day 1.


Minimum Physical Requirements:

  • Talking on phone/in person; frequently (34-100%)
  • Sitting; frequently (34-100%)
  • Standing/Walking; frequently (34-100%)
  • Lifts objects weighing up to 25 pounds; occasionally (0-33%)
  • Typing on keyboard; occasionally (0-33%)




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