Job Description

Job Description The Clinical Research Coordinator (CRC) collaborates with investigators, research teams, clinical departments, IRBs, and sponsors to plan, implement, and manage clinical trials and research projects for the Common Spirit Health Research Institute. Responsibilities include participant recruitment, screening, enrollment, conducting protocol-required visits, data collection, and coordinating sponsor monitoring or federal audits. The CRC ensures compliance with federal and state regulations, institutional policies, and maintains accurate documentation, adverse event reporting, and study drug accountability. This role upholds quality standards and supports the mission and values of CommonSpirit Health through professional service and regulatory adherence. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: Skills and Requirements - Bachelors in a science or related field. A combination of education and/or additional job-related experience in lieu of the degree.  - 3 years of experience conducting clinical trials required; worked as primary research coordinator for at least 5 drug or device trials.  - 3 years of experience interacting with patients in a healthcare setting  - Experience using electronic data capture software and Clinical Trial Management Systems  - Certified Clinical Research Professional (CCRP), within 12 - months or  - BLS - Certified Clinical Research Professional (CCRP), within 12 - months or  - Certified Clinical Research Coordinator ACRP (CCRC-ACRP) within 12 - months or  - Certified Clinical Rearch Coordinator SCRA (CCRC-SCRA) within 12 - months or  - Certified Phlebotomy Technician (ANCC)

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