As the Clinical Research Operations Coordinator, you will coordinate the research efforts of multiple Principal Investigators (PIs) to ensure that all regulatory agency policies, procedures, practices and laws are observed. This position requires extensive experience in management of clinical research in a patient care, biostatistics or data management environment. The ideal candidate will be able to use independent judgment and experience to solve complex issue relating to the department’s clinical research studies. (CB)
BSN required. Must possess good working knowledge of Good Clinical Practice guidelines, IRB review and reporting requirements, and regulatory affairs.
Six (6) years related work experience, four (4) years of which must have been in clinical research.
Must possess a current Tennessee State Board of Nursing license if primary residence is Tennessee or a non-Nurse Licensure Compact state.
Must possess a current State Board of Nursing license in the state of primary residence if the state is a Nurse Licensure Compact state.
OTHER CREDENTIAL REQUIREMENTS:
Certified Clinical Research Professional (CCRP) from SoCRA or ACRP or must obtain within six (6) months of employment.
Continued employment is contingent on successful completion of certification within the first six (6) months of employment.
Must maintain by re-certification while in position.
Must maintain appropriate professional competencies and have appropriate training in the protection of human subjects during the first six (6) months in the position.
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