Engage in a variety of clinical research activities, including patient-oriented research, human subject studies, and laboratory procedures
Conduct standard complete blood count procedures for orthobiologic cases in a CLIA-accredited laboratory
Communicate effectively with several entities, physicians, and researchers
Lead clinical trials and ensure compliance with regulatory requirements
Maintain a thorough understanding of assigned human subject research protocols and focus on the biobanking initiative, investigator-initiated studies, and industry-sponsored research
Assist with day to day operations of clinical trials and studies
Review research protocol inclusion/exclusion criteria and confirm subject eligibility
Perform informed consent process
Collect, code, and analyze data obtained from research
Act as a Primary Coordinator on multiple trials/studies for Intermediate and Senior Levels
Assist with developing protocol-specific systems and documents including process flows and training manuals for Senior Level
Conduct laboratory tests and manage inventory

Bachelor’s degree in any field
A combination of education and related technical/paraprofessional experience may be substituted for the bachelor’s degree on a year for year basis
One (1) year clinical research or related experience
Two (2) years clinical research or related experience for Senior Level
Experience with electronic data capture systems (e.g., EMR or EHR and data management systems)
Knowledge and understanding of federal regulations and Good Clinical Practice (GCP) and Good Laboratory Practice
Additional certification (one of the following): CCRC – Certified Clinical Research Coordinator, CCRP – Certified Clinical Research Professional, CCRA – Certified Clinical Research Associate

Clinical Research Coordinator – Open Rank

Key skills