1. Spencer Jenkins, MSHCM
Curriculum Vitae
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30 San Carlos Avenue
New Orleans, LA 70121
504-920-0301
cojenx@me.com
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
Ochsner Clinic Foundation, New Orleans, LA
2007-2008 Clinical Research Coordinator
Ochsner Clinic Foundation, New Orleans, LA
2002-2006 Clinical Research Coordinator
Mississippi Neuropsychiatric Clinic, Madison, MS
2. Spencer Jenkins, MSHCM
Curriculum Vitae
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Personal Qualifications:
Knowledgeable in all areas of clinical trials including:
o Good Clinical Practice (CITI Course certification)
o Budgeting
o IRB protocol submissions
o On-going maintenance of essential documents, including 1572s, financial
disclosure forms, CVs, medical licenses and certifications
o IND safety reporting
o SAE reporting
o Informed consent documents
o Sponsor communication
o 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
protocol
o Collaboration with the investigator to create a complete and readable
informed consent
o 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 documentation
o Able to outline and write scholarly articles
o Meticulously attentive to detail
o 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 was conducted on the 29th and 30th of September,
2015. It revealed no regulatory deficiencies.
