Posted in Other 30+ days ago.
Short Description
1. |
Interfaces with research participants and determines effective strategies for recruiting and retaining research participants in long term clinical trials |
2. |
Interfaces with study sponsors and resolves issues related to study protocols |
3. |
Oversees data management for research projects |
4. |
Monitors and reports Serious Adverse Events |
5. |
Assists with regulatory submissions to the Institutional Review Board |
Education |
Required |
Preferred |
Special Considerations |
Education |
Required |
Preferred |
Special Considerations |
|
High School / GED |
Bachelor's Degree |
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Vocational / Technical School |
Master's Degree |
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Associate's Degree |
Doctorate Degree |
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Field of Study (Please Note) |
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Special Considerations Explained (if needed): |
Experience |
Required |
Preferred |
Special Considerations |
Experience |
Required |
Preferred |
Special Considerations |
|
0-2 years |
6-10 years |
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3-5 years |
10+ years |
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Special Considerations Explained (if needed): |
Licensure, Certification, and Registration |
Required |
Preferred |
Special Considerations |
|
Certified Clinical Research Professional |
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Special Considerations Explained (if needed): |
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Skills / Qualifications |
Required |
Preferred |
Communication - Ability to communicate with patients, visitors and coworkers |
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Scheduled Days / Hours: Monday-Friday 8:30am-5pm
American Water |
American Water |
American Water |