Role OverviewAssists with the coordination and implementation of assigned clinical research trials under the direct supervision of the Principal Investigator and senior study staff.
What You Will Do
Performs assigned activities related to clinical research studies, including screening participants for eligibility, obtaining informed consent, and documenting accurate participant records and study records.
Why It Might Be a Fit
Requires in-depth knowledge of protocol requirements and Good Clinical Practice (GCP) guidelines, as well as excellent verbal, written, interpersonal, and communication skills.
Requirements
- Bachelor's Degree (Required) or Associate's Degree with 4 years of healthcare or research-related experience (Required)
- Certification in Human Subjects Protection (CITI) (Required within 30 Days)
- Experience in a team setting (Preferred)
- Medical terminology or basic research terminology (Preferred proficiency)
- DOT/IATA Training (Preferred proficiency)
Benefits
- Dental insurance
- Vision insurance
- Health insurance
- Retirement plan
- Paid time off
- Travel reimbursement
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