*Clinical Trials Compliance Manager - University of Oklahoma : Job Details

Pay Competitive

Employment type Full-Time

Req#: 359941 !*!

OU Health Stephenson Cancer Center is Oklahomas only National Cancer Institute (NCI)-Designated Cancer Center, and one of only 71 NCI-Designated Cancer Centers in the United States. This highly competitive accreditation ensures that our patients receive the highest standard of care and have access to the most advanced cancer treatment options.

At the Stephenson Cancer Center, we have an exciting new job opportunity that could be right for you! The Clinical Trials Compliance Manager is responsible for all auditing of site-speci?c and a?liate clinical trials and investigator-initiated studies to ensure compliance with federal, sponsor, and internal guidelines. This position monitors protocol compliance and discusses with management protocol deviations and recommends appropriate process changes to enhance data quality. The Clinical Trials Compliance Manager collaborates with informatics and Database Analyst to ensure compliance with Health Insurance Portability and Accountability Act (HIPAA) requirements.

Duties:

• Responsible for all auditing of site-speci?c and a?liate clinical trials in compliance with federal, sponsor, and internal guidelines
• Develops and implements site auditing and informatics Standard Operating Procedures (SOPs) and provides critical input
• Monitors for protocol compliance to include but not limited to dosing, study procedures, assessment entries, study patient documents to identify protocol non-compliance, and develops action plans to address the de?ciencies
• Discusses protocol deviations with appropriate Clinical Trials sta? and management
• Formulates and recommends appropriate process changes to enhance data quality
• Ensures Clinical Trials O?ce (CTO) informatics and databases are compliant with HIPAA requirements
• Performs auditing of investigator-initiated studies in compliance with the Code of Federal Regulations (CFR) guidelines and internal standard operating policies and procedures
• Represents the site as point-of-contact for external auditors in all external auditing activities
• Performs systematic internal audits of studies in preparation for the enhancement of data quality and in preparation for external audits
• Trains and prepares sta? for external audits
• Coordinates preparation for audits with physicians, data management, pharmacy, and research nurses
• Ensures that data is ready for auditors and works directly with sta? and physicians to resolve outstanding clinical or data entry issues
• Implements standard operating policies and procedures for research record organization and storage
• Develops site- speci?c operational policies and procedures to ensure site compliance with CFR guidelines
• Performs training and educational programs to ensure clinical research sta? are trained in compliance with CFR quality guidelines
• Supervises auditing and informatics sta? to include hiring, training, evaluating, reprimanding, and terminating employees
• Evaluates recommendations and action plans from external audits and is responsible to make changes recommended by the audits
• Collaborates with other departments, physicians, and principal investigators to implement the recommended changes
• Updates the standard operating policies and procedures if needed
• Prepares study-speci?c reports of audit ?ndings and discusses with management and other sta?
• Performs various duties as needed to successfully ful?ll the function of the position
!*!

Education: Bachelors Degree

Experience: 60 months experience in clinical trial data management or regulatory compliance.

Equivalency/Substitution: Will accept 48 months clinical trial data management or regulatory compliance experience in lieu of the Bachelors Degree for a total of 108 months experience. Masters Degree and 36 months clinical trial data management or regulatory compliance experience

Skills:

• Advanced knowledge of clinic audit procedures
• Ability to communicate e?ectively
• Ability to identify protocol problems, analyze information, and evaluate results to solve problems
• Ability to develop constructive and cooperative working relationships with sta? and outside entities
• Ability to multitask
• Ability work as a team player and work independently
• Ability to supervise

Working Conditions:

• Physical: Sitting for long periods of time. Speaking and listening.
• Environmental: Standard Office Environment.

Equal Employment Opportunity Statement: The University of Oklahoma, in compliance with all applicable federal and state laws and regulations, does not discriminate on the basis of race, color, national origin, sex, sexual orientation, genetic information, gender identity, gender expression, age, religion, disability, political beliefs, or status as a veteran in any of its policies, practices, or procedures. This includes, but is not limited to, admissions, employment, financial aid, housing, services in educational programs or activities, and health care services that the University operates or provides.

Diversity Statement: The University of Oklahoma is committed to achieving a diverse, equitable, and inclusive university community by recognizing each person's unique contributions, background, and perspectives. The University of Oklahoma strives to cultivate a sense of belonging and emotional support for all, recognizing that fostering an inclusive environment for all is vital in the pursuit of academic and inclusive excellence in all aspects of our institutional mission.

The University of Oklahoma is a public research university in Norman, Oklahoma.

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