Quality Improvement and Compliance Monitor
Be among the first 25 applicants
VETERANS ARE ENCOURAGED TO APPLY
Responsibilities
Conducting for-cause audits authorized by the IRB or institutional official.
Writing reports and communicating findings with investigators, compliance committees, and appropriate parties.
Conducting education and training throughout the monitoring process with the ability to recommend for further training to the human research education committee.
Providing regulatory guidance to the NYSPI research community. Assisting with site or study-specific research self-assessments.
Qualifications
Previous experience as a member of a research team (i.e., study coordinator/research assistant)
Thorough knowledge of state and federal codes (Revised Common Rule, FDA, etc.) regarding research.
Considerable knowledge of Good Clinical Practice (GCP)
Certification as a Clinical Research Associate (CCRA) or SOCRA Certified Clinical Research Professional (CCRP)
Advanced computer/technical skills
Salary
$107,005 - $127,588
TO APPLY AND TO VIEW A FULL DETAILED JOB DESCRIPTION, PLEASE VISIT THE LINK BELOW