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Spencer Jenkins, MSHCM Curriculum Vitae ________________________________________________ ______________________________ 30 San Carlos Avenue New Orleans, LA 70121 504-920-0301 [email protected] Education: M.S. Health Care Management University of New Orleans, New Orleans, LA Graduate Studies Vanderbilt University, Nashville, TN B.A. French Literature The University of the South, Sewanee, TN Honors: Beta Gamma Sigma International Honor Society for Business Students Certifications: Certificate, Responsible Conduct of Research CITI Program, University of Miami Profession Research Experience: 2008-Present Regulatory Coordinator – Oncology Clinical Trials Ochsner Cancer Institute

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Page 1: CV_Jenkins_22nov15_n BI

Spencer Jenkins, MSHCMCurriculum Vitae

______________________________________________________________________________30 San Carlos AvenueNew Orleans, LA 70121 [email protected]

Education: M.S. Health Care ManagementUniversity of New Orleans, New Orleans, LA

Graduate StudiesVanderbilt University, Nashville, TN

B.A. French LiteratureThe University of the South, Sewanee, TN

Honors: Beta Gamma SigmaInternational Honor Society for Business Students

Certifications: Certificate, Responsible Conduct of ResearchCITI Program, University of Miami

Profession Research Experience:

2008-Present Regulatory Coordinator – Oncology Clinical TrialsOchsner Cancer InstituteOchsner Clinic Foundation, New Orleans, LA

2007-2008 Clinical Research CoordinatorOchsner Clinic Foundation, New Orleans, LA

2002-2006 Clinical Research CoordinatorMississippi Neuropsychiatric Clinic, Madison, MS

Personal Qualifications:

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Spencer Jenkins, MSHCMCurriculum Vitae

______________________________________________________________________________ Knowledgeable in all areas of clinical trials including:

o Good Clinical Practice (CITI Course certification)o Budgetingo IRB protocol submissionso On-going maintenance of essential documents, including 1572s, financial

disclosure forms, CVs, medical licenses and certificationso IND safety reportingo SAE reportingo Informed consent documentso Sponsor communicationo Able to establish strong rapport with clinical trial participants

Experienced in investigator-initiated trials including:o Assisting the investigator in the preparation, editing, and submission of the

protocolo Collaboration with the investigator to create a complete and readable

informed consento Communication with the FDA and OBA in the form of annual reports for

investigator-initiated trials. Extensive experience in the field of scholarship:

o Able to research topics through a variety of search engines and online inter-library loan services

o Proficient in source documentationo Able to outline and write scholarly articleso Meticulously attentive to detailo Knowledgeable about grammar and punctuation

Good computer skills, particularly in the use of Microsoft Word and Excel spreadsheets.

As a CRC, I had extensive interaction with patients, particularly when I was working in psychiatry . I completed encounter notes, entered information into patient charts, and completed CRFs. I have also audited charts in other departments in preparation for external audits.

In my present position, I have been personally responsible for the initial completion and maintenance of all documentation for over 450 clinical trials. I believe that is a strong indication of my dedication to my work, to my ability to work independently, and to my ability to prioritize and organize a considerable volume of tasks.

A 3rd-party audit of one of my studies , commissioned by Boehringer Ingelheim, was conducted on the 29th and 30th of September, 2015. It revealed no regulatory deficiencies.

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Spencer Jenkins, MSHCMCurriculum Vitae

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