Research Development Assoc
On-siteSarasota, Florida, United States
Job Summary
Conduct independent-driven research by recommending and utilizing effective statistical methodology and data management strategies for project creation, completion, and analysis. Oversee research and administrative strategies for the successful management of research publications for Sarasota Memorial Health Care System in accordance with good clinical practice and FDA regulations. Maintain a valid driver's license and complete Human Subject Protection Training within thirty days of hire. This role supports the Research Institute's clinical trial creation and manuscript development while requiring one year of clinical experience and Clinical Research Professional certification.
Required Qualifications
- one (1) year of clinical experience preferably within a research setting
- certification as a Clinical Research Professional (or obtained within one (1) year of hire)
- completion of Human Subject Protection Training (or obtained within thirty (30) days of hire)
- Valid Driver's License
Desired Qualifications
- demonstrated ability to assist with independent clinical trial creation
- demonstrated ability to initiate work without supervision and work independently
- demonstrated knowledge of and willingness to learn medical manuscript
- demonstrated knowledge of commonly used computer applications, including database and data mining
- demonstrated knowledge of statistics and research grant processes
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