Associate Clinical Research Coordinator - RESEARCH

The Clinical Research Coordinator 1(CRC1) is responsible for coordinating and maintaining diverse activities related to clinical cancer research. This includes but is not limited to: patient eligibility; registration/enrollment; data compilation, abstraction, and submission; study evaluation; quality control; and patient follow-up. The CRC1 interacts closely with institutional investigators, industry sponsors, contract research organizations, NCTN research bases, clinic staff, laboratory staff, and pathology staff. The CRC1 collaborates with fellow clinical research staff throughout the duration of the study to ensure high quality and efficient study conduct.

Providence caregivers are not simply valued – they’re invaluable. Join our team at Kadlec Regional Medical Center and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them.

Required Qualifications:

• Associate's Degree or equivalent educ/experience


• 2 years Microsoft Office Suite experience

Preferred Qualifications:

• Bachelor's Degree in healthcare or related field or equivalent educ/experience


• Upon hire: Certified Clinical Research Coordinator (CCRC) - Association of Clinical Research Professionals or similar professional research certification


• 2 years human subject research or healthcare experience


• Experience working with electronic medical records (EPIC)


• Experience with Oncology and/or Radiation Oncology

Why Join Providence? 

Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security.  We take care of you, so you can focus on delivering our mission of providing safe, compassionate care.