Facility:
Dayton Children’s - Main Campus
Department:
Clinical Research Operations
Schedule:
Full time
Hours:
40
Job Details:
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. They 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.
Department Specific Job Details:
Required:
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
Preferred:
Professional Certification in Clinical Research or willing to work towards obtaining certification within 2 years of hire

Talroo

Education Requirements:
Associates (Required)
Certification/License Requirements

Please refer the Job description for details