Description
Passionate, hard-working, intelligent, leader, compassionate, organized
Work Experience
COMPANY | POSITION HELD | DATES WORKED |
---|---|---|
(Confidential) | (Confidential) | 4/2008 - Present |
University of Iowa Clinical Trials Statistical and Data Management Center | (Confidential) | 7/2005 - 4/2008 |
University of Iowa Human Subjects Office | (Confidential) | 4/2002 - 6/2005 |
University of Iowa Dept. of Pharmaceutical Care | (Confidential) | 11/1999 - 4/2002 |
Education
SCHOOL | MAJOR | YEAR | DEGREE |
---|---|---|---|
University of Iowa | Religion-Ethics | 2001 | Master Degree |
Concordia College, Moorhead, MN | Music; Pre-medicine curriculum | 1992 | Bachelor Degree |
Accomplishments
Highlights:
Companies I like:
I would enjoy working with any CRO or Sponsor who values and rewards excellence and a strong work ethic from their employees.
Job Skills
Keywords
Responsibilities
In my current position, I am responsible for obtaining and reviewing all documents from our participating sites' Regulatory Binders. I am also responsible for providing GCP training to investigators and reviewing IRB requirements at Site Initiation Visits.