Clinical Research Coordinator

Clinical Research Coordinator

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.

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