Clinical Research Coordinator

Dayton Children's Hospital

11d•Onsite

About The Position

The Clinical Research Coordinator will perform clinical research activities under the general direction of the Clinical Research Supervisor/Manager and a Principal Investigator (PI) while adhering to International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) Guidelines. S/he will perform tasks, including but not limited to: site feasibility, preparation, patient screening and recruitment, patient enrollment, conducting study visits, completing and ensuring the quality of case report forms, maintaining source documents, and ensuring site quality. This position will also require familiarity with IRB submissions and regulatory processes. Most important of all, the Clinical Research Coordinator will ensure the safety and well-being of all study participants throughout all study activities. At Dayton Children's, we believe that each moment counts with our patients, families, and with each other. We are moving at a fast pace and are looking for the right talent for our team at Dayton Children's. We want people who embody our values and want to become a part of the Dayton Children's difference. If this is you, apply today! Our values: We commit to safety - We ensure every action and decision prioritizes the safety of patients, families, and employees. We serve with compassion - We bring generosity, empathy, and kindness to all interactions. We own every moment - We take pride in everything we do. We’re better together - We collaborate, communicate, and support one another to deliver optimal care. We innovate with purpose - We adapt and change to improve pediatric care, for today and tomorrow. We value and respect each person - We create an inclusive space where everyone feels welcome and respected. Dayton Children’s is proud to be an Equal Opportunity Employer that values diversity and will not discriminate against minorities, women, protected veterans, individuals with disabilities, or based on age, color, gender identity, national origin, race, religion, sex, sexual orientation, or transgender status.

Requirements

Associates Degree
1-2 years of Research Assistant, Research Coordinator, or Regulatory Coordinator experience.
Working knowledge of medical terminology and research terms
Working knowledge of PCs, word processing, excel and data management software.
Tech-savviness and willingness to learn new software applications

Nice To Haves

Professional Certification in Clinical Research or willing to work towards obtaining certification within 2 years of hire
Education: Bachelors/Masters degree preferred.

Responsibilities

site feasibility
preparation
patient screening and recruitment
patient enrollment
conducting study visits
completing and ensuring the quality of case report forms
maintaining source documents
ensuring site quality
IRB submissions and regulatory processes
ensure the safety and well-being of all study participants throughout all study activities