About The Role

Our patients are our number one priority! We're committed to giving children back their childhood!

Dallas - Hospital

Assist in preparation and maintenance of research and regulatory documents for Research Advisory Panel, Institutional Review Board, and other regulatory agencies
Identify eligible patients and obtain informed consent
Collect, validate, and enter data into research databases or spreadsheets
Assist with the preparation and submission of abstracts, journal manuscripts and other presentations as needed
Supervise summer students/interns and contribute to the training of Level I and new Level II Research Coordinators

Bachelor’s Degree required; Master’s Degree preferred
3-5 years of experience in clinical research
CCRP certification
Must have proficient computer skills in a Windows environment; spreadsheet software knowledge a plus
Ability to effectively communicate and collaborate with other health professionals as well as substantial interpersonal skills necessary to communicate with patients, their families, and the community.
Critical thinking skills and time management skills are required; must have the ability to multi-task and work with minimal supervision