Clinical Research Coord I

2 weeks ago

Dayton, United States Kettering Health Full time

Overview:

Kettering Health is a not-for-profit system of 13 medical centers and more than 120 outpatient facilities serving southwest Ohio. We are committed to transforming the health care experience with high-quality care for every stage of life. Our service-oriented mission is in action every day, whether its by providing care in our facilities, training the next generation of health care professionals, or serving others through international outreach.

Campus Overview:

Kettering Health Main Campus

  • Kettering Health Main Campus, formerly Kettering Medical Center, is the flagship hospital of Kettering Health and has been serving Kettering, Ohio and the Greater Dayton area since 1964.
  • The facility includes the Benjamin and Marian Schuster Heart Hospital, maternity service with a level III neonatal intensive care unit (NICU), and level II Emergency Care.
  • In 2020, KH Main Campus received an A from the Leapfrog Group, a national patient safety watchdog, ranking among the safest hospitals in the United States.
  • Received 4 Star Baby-Friendly Hospital status by the Ohio Hospital Association.
  • Awarded as one of the 50 Top Cardiovascular Hospitals by IBM Watson Health in 2020.
  • Kettering received the Outstanding Patient Experience Award by Healthgrades (2017-2019).
  • Accredited by the American College of Emergency Physicians as a Level 3 Geriatric Emergency Department.
  • 465-bed hospital (includes newborn beds)
Responsibilities & Requirements:

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 CRCs 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.

Preferred Qualifications:
  • Bachelor's Degree required.
    • Preffered 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.

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.

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