Clinical Research Data Specialist

Overview:

The Clinical Research Data Specialist is responsible for the building and maintenance of clinical research projects in clinical research management systems. This includes, creating visit and procedure calendars and entering budget and payment information.

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:

Supports technical needs of end users in a timely manner by creating Study Protocols in clinical research management system, including related Calendars, Procedures, Visits, Forms, Budgets, etc.

Demonstrates a working knowledge of the components of a clinical research protocol; can identify procedural components to be budgeted.

Collaborates with Feasibility Coordinators and study teams regarding data requirements and accuracy for studies of varying complexity

Participates in data migration-related activities and data entry related to study protocol requirements.

Works with Feasibility Coordinator and/or Clinical Research Business Operations Team Lead to ensure issues are resolved in a timely manner.

Ensures accuracy of calendars, budgets and payment information to ensure compliance with billing regulations and to meet organizational reporting needs.

Ensures accuracy and completeness of payment terms to maximize revenue capture.

Assists builds in other clinical research management systems i.e., eRegulatory, eConsent, RedCap, Smartsheets etc.

Qualifications:

Education: Bachelor's degree preferred or 2-3 years of equivalent experience.

Skills:

Accountability in task ownership and solution-oriented work approach

Ability to work independently using initiative and good judgment

Working knowledge in the use of information technology

Strong organizational skills including attention to detail and multi-tasking

Ability to filter information, discern importance and efficiently execute tasks

Excellent verbal and written communication skills.

Experience in an applied data management or services role. 1-2 years experience in clinical research preferred.

The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this classification. It is not to be construed as an exhaustive list of duties performed by the individual so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under his/her supervision.

EOE M/F/Disability/Vet

Permanent