Our patients are our number one priority! We're committed to giving children back their childhood!
Requirements
Bachelor’s Degree required
3-5 years of experience in clinical research
CCRP certification
Must have proficient computer skills in a Windows environment
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
Nice To Haves
Master’s Degree preferred
spreadsheet software knowledge a plus
Responsibilities
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