Role OverviewResponsible for managing a clinical study involving multiple sites around the world. Leading the efforts on selecting the sites, testing the sites capabilities to ensure long-term compliance, engaging in contractual agreements with the sites, and training the staff at each site with respect to the study protocol and data upload to the web-based data collection system.
What You Will Do
Manage a clinical study, engage potential sites, train site coordinators, monitor site coordinators, generate and maintain standard operating procedures, communicate project progress, troubleshoot problems, prepare reports, and present progress at research staff meetings.
Why It Might Be a Fit
Must be self-motivated, able to work independently, have excellent critical thinking skills, and strong organizational skills. Familiarity with grant submissions processes and various grant award mechanisms is also required.
Requirements
- Bachelor's Degree in a Related Field of Study
- 3-5 years of Research Related Experience
- Excellent critical thinking skills
- Ability to work independently
- Good verbal and written communication skills
- Proficiency in Word, Powerpoint, Excel
- Ability to make independent effective decisions
- Strong organizational skills
- Demonstrated analytical skills to problem solve effectively
- Familiarity with grant submissions processes and various grant award mechanisms
- Strong computer proficiency and database management skills
Benefits
- Comprehensive benefits
- Career advancement opportunities
- Differentials
- Premiums
- Bonuses
- Recognition programs
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