Assist in the management of multiple clinical trials and responsibilities in specific research area. Coordinate the screening of patients, subject enrollment, collection and storage of biological samples and related study documents, and collection of clinical data.
Requirements
- Bachelor of Science and 1 to 2 years of experience
- GCP knowledge
- Federal regulations and guidance documents knowledge
- IRB filings and inquiries knowledge
- Manuscript, grant proposal, and research presentation preparation
Benefits
- Comprehensive medical, prescription, behavioral health, dental, vision, and life insurance benefits
- Flexible spending accounts for health care and dependent care expenses
- Tuition assistance for self and family members
- Generous retirement plans
- Long-term care insurance
- Wellness and work-life resources
- Professional and personal development resources
- University resources and cultural activities
- Discounts and special services
- Flexible work hours