Clinical Research Coordinator II – RI Emer Medicine

Clinical Research Coordinator II – RI Emer Medicine
Requisition ID
2024-52996
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 Childrens 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 Childrens 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.
Were 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 well 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 Childrens badge what they do for a living. Theyll tell you its More Than a Job. Its a calling. Its 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 Childrens Hospital. A Place to Be Proud.
Responsibilities
Performs research activities as outlined in study protocols; screen, approach, consent and collect data according to protocol
Provides in-person and electronic updates to EM Team Lead and Study PIs (as needed)
Creates source documents that facilitate systematic data collection and/or aid in protocol execution and management
Assists in the development and implementation of study trainings and is able to provide assistance to EM Research Team members during training periods
Acts as a peer reviewer for data collection completed by EM Research Team
Ensures protection of human subjects rights through IRB regulations
Responsible for regulatory/IRB issues after a study has been initiated by the study sponsor
Creates IRB submissions for study oversight including but not limited to Study Modifications, Continuing Reviews, and External Updates
Communicates any concerns or questions with the EM Team Lead, EM Research Project Manager, EM Research Director and Study PIs as needed
Assists the EM Team Lead to delegate study tasks to EM Research Team members
All other duties as assigned
Qualifications
Reports to: EM Research Coordinator Team Lead
Masters degree preferred
Experience with informed consent/ research enrollment
Some evening and weekend hours required
Excellent communication and organizational skills to effectively interact with medical staff, consultants, external professionals, administrators, and employees at all levels.
Excellent skills in writing, communications, and presentation graphics knowledge required
Knowledge and experience in study management preferred
Significant contact with medical staff, outside vendors and community representatives
Minimum physical requirements:
Talking on phone/in