Working Title/Rank:

Director

Position Category:

Research Professionals

Recruitment ID:

2502205

Position ID:

1001805

Salary Range:

Salary Dependent upon Qualifications

FT/PT:

Full Time

Department:

Clinical Trials

Application Deadline:

Open until Filled

Proposed Start Date:

03/01/2012

 

Position Summary:

The Director of the Office of Clinical Trials (OCT) at the University of North Carolina at Chapel Hill (UNC-CH) is responsible for the daily management and operations of clinical trial financial, regulatory and compliance services to all UNC-CH. The Director will oversee and assume responsibility for clinical trial billing compliance, appropriate identification of charges billable to third party payers, contract negotiation/budget development, feasibility analysis, regulatory support, and ongoing post award management and monitoring for clinical trials. This position reports directly to the Associate Vice Chancellor for Research, and will work in close collaboration with the Directors of Research Compliance, Office of Sponsored Research, the Office of Human Research Ethics (where the Institutional Review Boards are located), and UNC Health Care. Other areas of responsibility include: Ensure the creation and quality review of Medicare Coverage Analyses for all clinical trials Oversee the process to register all clinical trials and link all clinical trial participants in the institution's central clinical trial management system(s); and work with campus units to ensure that clinical research income is properly received and accounted for in institutional financial systems. Ensure that clinical trials are registered in the federal clinicaltrials.gov repository, as required. Facilitate timely and appropriate communication with Principal Investigators and Research Nurses/Coordinators on all aspects of clinical research administration Expand the regulatory Monitoring Program and the Research Subject Advocacy Program to ensure compliance with Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP) regulations and the Informed Consent process. Develop, organize, and/or conduct clinical research administration and regulatory educational programs Lead continuous process and operational improvement initiatives to reduce cycle-times, improve overall compliance posture, and remove unnecessary administrative burdens. Establish key operational metrics and publish periodic performance reports to stakeholder groups. The Director will also ensure that the office provides knowledgeable, friendly, professional and timely support to faculty and staff. This individual is also responsible for safeguarding UNC-CH's interests by assuring compliance with various Federal and State regulations and laws, as well as Institutional policies associated with management of clinical trials. This position will be responsible for developing, in consultation with the Associate Vice Chancellor for Research and the campus community, policies and procedures relating to corporate sponsored clinical trials. The ability to manage a diverse staff of clinical trials experts and have a deep understanding of the clinical trial process and the impact of OCT operations on that process is required

 

Education Requirements:

Graduate degree preferred, Bachelor's degree required with a minimum of 5 years of clinical research, or the equivalent, and prior experience supervising staff.

 

Qualifications and Experience:

A strong clinical research regulatory background as well as excellent written and oral communication skills, including the ability to speak in front of groups is essential. Knowledge of clinical research regulations and Federal and State law governing clinical research and tax-exempt organizations is required. Knowledge of Federal healthcare and commercial insurer billing regulations is strongly desired. Knowledge of computer databases and general computing software is essential, and experience with clinical trial management systems is desired.

 

Special Instructions:

Applicants need to submit a letter and CV and apply online at http://jobs.unc.edu/2502205

 

Contact:

If you experience any problems accessing the system or have questions about the application process, please contact the University's Equal Employment Opportunity Office at (919) 966-3576 or send an email toxxxxxx@unc.edu.

 

If you have any questions about the job requirements or the hiring department, please contact Jo Ann Gustafson, Director of Operations, xxxxxx@unc.edu.

**********************************************************************

Aylin A. Regulski M.S., J.D.

Interim Director, Office of Clinical Trials                                        

Description: Description: Condensed Well

Bioinformatics Bldg., Room 1109A

130 Mason Farm Road, CB #1651

Chapel Hill, NC   27599-1651

 

CONFIDENTIALITY NOTE

The information contained in this message is legally privileged and confidential information intended only for the use of the individual or entity named above.  If the reader of this message is not the intended recipient or the employee or agent responsible for delivering this message to the intended recipient, you are hereby notified that any dissemination, distribution or copying of this communication is strictly prohibited.  If you have received this communication in error, please notify us immediately by telephone.

 

 

 

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