Dedicated Clinical Research Coordinator experienced in complying with study protocols, standard operating procedures and good clinical practices. Practiced problem-solver with strong attention to detail. Prepared to offer 5 years' experience in the field and take on a fast-paced position.
Overview
5
5
years of professional experience
Work History
Study Coordinator
Dechra Veterinary Products
Leawood, KS
04.2019 - Current
Gathered and reviewed study data.
Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
Ensured that studies were conducted in accordance with the scientific design and timelines provided.
Conducted screening interviews to determine eligibility of possible subjects.
Placed orders for supplies and study drug to be used in studies.
Collaborated with others to discuss new opportunities.
Achieved cost-savings by developing functional solutions to problems.
Performed data entry to ensure a high-quality data set.
Compared data logs against written records to verify accuracy of electronic records, alerting management to discrepancies indicating poor data entry execution.
Education
Bachelor of Science - Animal Science
Kansas State University
Manhattan, KS
08-2018
Skills
Protocol development
Documentation requirements
Schedule Coordination
Records Management
Enrollment coordination
Proficient in Microsoft Word, Excel, PowerPoint and Outlook
Attention to detail and ability to adhere to project deadlines
Ability to multitask
References
References available upon request.
Timeline
Study Coordinator
Dechra Veterinary Products
04.2019 - Current
Bachelor of Science - Animal Science
Kansas State University
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