A company is looking for a Clinical Research Coordinator I.
Key Responsibilities
Conducts clinical trials in compliance with FDA regulations and ICH guidelines
Maintains subject research records and manages treatment and follow-up schedules
Obtains informed consent and assists with patient education regarding study protocols
Required Qualifications, Training, and Education
Bachelor of Science degree or equivalent combination of education and research experience
Certification from ACRP or SOCRA required within 2 years of employment
Current AHA Basic Life Support certification for Healthcare Providers
No prior experience required; preferred experience includes working as a Clinical Research Coordinator
Basic knowledge of clinical tasks and experience with multidisciplinary teams preferred
Clinical Research Coordinator • Lincoln, Nebraska, United States