The position requires coordinating the screening, enrollment, and data reporting for patients enrolled in clinical research studies while ensuring the rights and well-being of human subjects are protected
Job Summary
The position requires coordinating the screening, enrollment, and data reporting for patients enrolled in clinical research studies while ensuring the rights and well-being of human subjects are protected.
Candidates must verify that trial conduct complies with approved protocols, Good Clinical Practice (GCP), and applicable sponsor and regulatory requirements.
The role involves obtaining informed consent, facilitating study visits, and collaborating with pharmacists and laboratory personnel to manage drug inventory and specimen shipping.
Matching Summary
The position requires coordinating the screening, enrollment, and data reporting for patients enrolled in clinical research studies while ensuring the rights and well-being of human subjects are protected.
Skills & Requirements
Must-have
Bachelor of Science in science discipline
Good Clinical Practice (GCP) compliance
Informed consent acquisition
Source document verification
Study eligibility verification
Nice-to-have
Collaboration with clinical staff
Cost-effective resource use
Exceptional customer service
Self-directed professional development
Process improvement suggestions
Key Requirements
Bachelor of Science degree in a science discipline