Expert Details
Energy and Power Industries
ID: 727054
Kentucky, USA
IP and C provides services from installing database software to organizing and setting into place an entire tech transfer office. They train and provide professional standard operating procedures for all stages of the departments/offices and can also provide further assistance as the department grows and prospers.
Education
Year | Degree | Subject | Institution |
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Year: 2009 | Degree: PhD | Subject: Analytical Chemistry | Institution: University of Kentucky |
Year: 2006 | Degree: BA | Subject: Chemistry | Institution: Berea College |
Work History
Years | Employer | Title | Department |
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Years: 2009 to Present | Employer: Undisclosed | Title: Owner and Consultant | Department: |
Responsibilities:Available upon request. |
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Years | Employer | Title | Department |
Years: 2009 to 2009 | Employer: University of Kentucky | Title: Student Employee | Department: Economic Development |
Responsibilities:Expert was responsible for converting the tech transfer office from a paper system to an all electronic system. He researched the workings of the department and tasks that all employees were responsible for in order to develop standard operating procedures for each step of the process. Each step of the department's workings was incorporated into the electronic system to keep record of every step of the technology transfer. |
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Years | Employer | Title | Department |
Years: 2008 to Present | Employer: Undisclosed | Title: Analytical Consultant | Department: |
Responsibilities:Expert was in charge of developing software to control prototype instrumentation that was designed to monitor the quality of water. The software was designed to connect to the instrument, control flow rates and valves, collect data, and perform all data analysis needed to find amounts of contaminants. |
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Years | Employer | Title | Department |
Years: 2008 to Present | Employer: Undisclosed | Title: Analytical Consultant | Department: |
Responsibilities:Expert was responsible for developing SOPs for the preparation of preservatives for a phase 3 clinical trial. He abided by FDA regulations in the preparation, storage and transportation of the preservatives. He developed standard operating procedures for combining the preservatives with the drug being tested in the clinical trial. He was also responsible for data analysis and interpretation regarding phase 2 clinical trial data. |