Senior Clinical Research Nurse

Responsibilities

• Lead and coordinate complex clinical studies within an academic medical environment.
• Manage participant recruitment, informed consent, and study procedures ensuring compliance with protocols.
• Oversee data collection, regulatory documentation, and adherence to Good Clinical Practice (GCP) standards.
• Monitor participant safety, report adverse events, and ensure high standards of patient care.
• Collaborate with investigators, clinicians, and community partners to support innovative research.
• Mentor junior staff and contribute to improving health outcomes for diverse populations.

Qualifications & Skills

• Experience in managing clinical studies and participant interactions.
• Knowledge of regulatory requirements and GCP compliance.
• Strong communication and collaboration skills.
• Ability to oversee data collection and ensure protocol adherence.
• Commitment to high-quality patient care and research excellence.