Clinical Research Coordinator - Laboratory of Regulatory Biology
About The Position
The Clinical Research Coordinator position will be responsible to participate and assist on all human studies in the RBIO-P lab, including, but not limited to, projects such as the "Influence of time-restricted eating (TRE) on circadian regulation of glucose homeostasis and mitochondrial function in patients with Metabolic Syndrome (TIMET 2.0), and the "Optimization of Chrononutrition to Reduce the Risk of Disease in Shift Workers." This role supports the labs’ initiative to investigate the effect of time-restricted eating in improving health. This position is responsible for supporting ongoing clinical trials and other duties as assigned.
Requirements
- Minimum 2 years’ experience, or equivalent combination of education and experience required.
- Bachelor's degree in Biological Sciences or related scientific discipline required. A minimum of 4 years of experience in a scientific role is required for consideration of a Bachelor's degree in a different discipline.
- Computer skills required: Microsoft Office.
Responsibilities
- Participant recruitment
- Running patient visits for clinical trials
- Monitoring patient participation
- Follow-up with study patients
- Preparing for study visits
- Data collection and entry
- Data and study sample management
- Data analysis (sleep scoring, nutritional analysis, etc.)
- Ordering supplies & running study related errands
- Other Administrative tasks for study data organization
- May require travel; reliable mode of transportation (required)
- Performs other related duties as assigned
Benefits
- medical
- dental
- vision
- retirement
- paid time off
- tuition reimbursement
- patient advocacy services
- transit/parking program
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
