Principal Clinical Research Coordinator
Behavioral Health Market Context
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Job Description
aining, and Education
Bachelor's degree in science, health, or a related field from an accredited university
5-7 years of research or relevant experience
Experience with CTMS, EMR, and eRegulatory Systems
Working knowledge of clinical trials and relevant regulations
Good Clinical Practice (GCP) and Human Subjects Protection (HSP) certifications required within specified timeframes
Bachelor's degree in science, health, or a related field from an accredited university
5-7 years of research or relevant experience
Experience with CTMS, EMR, and eRegulatory Systems
Working knowledge of clinical trials and relevant regulations
Good Clinical Practice (GCP) and Human Subjects Protection (HSP) certifications required within specified timeframes
Qualifications
- •Bachelor's degree in science, health, or a related field from an accredited university
- •5-7 years of research or relevant experience
- •Experience with CTMS, EMR, and eRegulatory Systems
- •Working knowledge of clinical trials and relevant regulations
- •Good Clinical Practice (GCP) and Human Subjects Protection (HSP) certifications required within specified timeframes
Benefits
Responsibilities
- •Serve as the primary point of contact between study sponsors, investigators, and research teams
- •Oversee operational execution of studies, including patient registration and study close-out activities
- •Ensure regulatory compliance and accurate documentation across various systems