The Clinical Research Coordinator I will assist various Principal Investigators, through delegated authority, with conducting clinical trials per Federal, State and Institutional guidelines.

  Learns knowledge of departmental functions through reading literature, attending workshops, seminars and conferences, and by participating in professional organizations

 Learns to conduct audits of research studies to check the accuracy, integrity and consistency of research studies

 Learns to coordinate study-monitoring visits

Assists in the development of research study budgets for new clinical trials, and helps ensure that appropriate billing or charging mechanisms are in place for research charges related to the research study

 Learns to coordinate research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met

Assists with regulatory compliance including assisting with preparing IRB materials for approval of protocol amendments, submitting Investigational New Drug (IND) Safety

 The ideal Clinical Research Coordinator I candidate is someone who is able to learn to coordinate implementation of various protocols for assigned research projects with appropriate departments throughout Baylor Scott and White Health by interacting with Principal Investigators and Clinical Managers/Supervisors, providing in-service education for healthcare professionals and working with Pharmacy to ensure a smooth project flow.