CLIN RES MONITORING SPEC
Duties: Reporting to the Chief Compliance Officer- Clinical Research, Abramson Cancer Center Department of Operations, Compliance and Monitoring (DOCM), responsible for scheduling, coordinating and conducting monitoring and/or auditing of all oncology studies being conducted within the Abramson Cancer Center as well as assisting with corrective actions and training related to research compliance, quality control and quality assurance. The Monitoring Specialist will follow all DOCM policies and procedures as well as have a thorough understanding of federal and local policies and guidance for the conduct of clinical research.
Position is contingent on continued funding.
Qualifications: BSN/RN or Bachelors degree and at least 3 years of experience as a clinical research nurse, clinical coordinator or clinical project manage, or equivalent combination of education and experience, are required. Experiences as research monitor/auditor is a plus. The appropriate candidate will possess a strong knowledge of GCP and the regulations related to IND/IDE. Must understand the principles of Quality Control and Quality Assurance as well as the federal, local and institutional regulations as they apply to the conduct of human subjects research. Must be highly skilled in MS Word and Excel applications, understand medical records/patient charts organization and terminology; detail oriented; excellent organizational and some management skills in a very diverse setting; ability to exercise discretion in working with highly confidential and sensitive information; must be able to multi-task and prioritize; must be able to work under pressure and exercise mature judgment; resourcefulness and imitative Applicants without the minimum qualifications will not be considered. CLINICAL RESEARCH EXPERIENCE IS A MUST
Reference Number: 40-26694
Salary Grade: 027
Employment Type: Exempt
Org: CC-Cancer Center
Job Family: I-Technical/Professional Research