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Informed Consent

Healthcare and Medical

Informed consent is the ethical and legal principle requiring that individuals be given clear, adequate information about a procedure, study, or treatment's risks and benefits before agreeing to participate. It's central to medical practice, clinical research, and human-subjects research, ensuring autonomy and voluntary participation. Healthcare providers, researchers, and ethics boards rely on informed consent processes to protect patient and participant rights.

Open roles requiring Informed Consent (1)

Research Nurse - Rheumatology

Cleveland Clinic

Full-time · Cleveland, OH

A clinical research role supporting rheumatology studies at Cleveland Clinic, where you'll manage trials from setup through completion, oversee patient safety and consent, and coordinate with physicians and sponsors. This suits nurses with clinical experience who want to shift from direct care into research operations and protocol management.

Listed on Cleveland Clinic’s careers site · Apply there ↗

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