Clinical Research Coord I - Innovate and Research in Kettering, Ohio at Kettering Health

Kettering Health is a not-for-profit system of 14 medical centers and more than 120 outpatient facilities serving southwest Ohio. Our mission is to live God’s love by promoting and restoring health. Our commitment to our patients is to help individuals be their best. With that context, safety is our top priority. We provide an integrated system of healthcare experts committed to providing exceptional care.

The Clinical Research Coordinator I (CRC I) is a professional with clinical research expertise preferred. Under the supervision of the Manager, Innovation, Research & Grants at KHN, the CRC I will collaborate with physicians and other healthcare providers, scientists, administration, the Institutional Review Board, Sponsors, and the Food and Drug Administration (FDA). The CRC I is responsible for assisting the Investigator in accomplishing successful research trials. The CRC I is expected to adhere to Good Clinical Practice (GCP) guidelines as set forth by the Federal regulations. The CRC I will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring of the subjects participating in the research study. The CRC I is responsible for all data reporting via source documents including adverse event reporting. Maintenance of complete regulatory files will be coordinated with the Regulatory Documentation Specialist (RDS). Depending on the requirements of a specific protocol, other duties may be assigned based upon the CRC’s qualification, training, experience and licensure, when applicable. The CRC I will adhere to policies of the Innovation, Research & Grants related to compliance of Federal regulatory issues, education, training, and GCP.

Job Requirements:

• Bachelor's Degree required
• Must be able to read and write English and follow oral and written directions. Must be able to collaborate in work projects and possess the ability to manage multiple project priorities. Must be able to work independently, collect data accurately, and complete tasks in a timely manner.
  CPR basic life support certification is required.

Job Responsibilities:

• This individual must be able to work independently under limited supervision, while maintaining excellent communication between the principal investigator(s) and all staff involved in any aspect of approved research projects.

• Preffered degree in Science Medical Field.
• Preferred to have 1-2 years of Clinical Research experience (patient oriented).
  • Recent graduates are accepted if they have schooling involved in field.