Role OverviewServe as a resource for conducting clinical trials, develop and implement associated projects, and collaborate with others to ensure proper progress and completion of studies.
What You Will Do
Collect and process specimens, coordinate regulatory activities, oversee data entry and validation, and assist in data analysis.
Why It Might Be a Fit
This role requires a strong understanding of clinical research practices, regulatory compliance, and data management. The ideal candidate will have experience in a related field and be certified as a Clinical Research Coordinator.
Requirements
- Bachelor's degree in a related field
- 1 year of directly related work experience
- Master's degree in a related field
- 3 years of experience in a related job discipline
- Certified Clinical Research Coordinator within 18 months of external hire date
Benefits
- Dental insurance
- Vision insurance
- Health insurance
- Retirement plan
- Paid time off
- Comprehensive job description provided upon request
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