Clinical Trials Research Nurse – Diabetes Center

Columbia University in the City of New York; New York (NY); Híbrido; USD 95 000 - 140 000; Tempo integral

Resumo da oferta

The Naomi Berrie Diabetes Center Research Nurse at Columbia University Irving Medical Center coordinates recruitment, enrollment, and direct care for clinical trial participants. You will work with pediatric and adult teams, perform phlebotomy, IV placement, and study drug administration, and ensure protocol adherence.

Responsibilities include consent discussions, scheduling visits, regulatory document preparation, and cross‑functional collaboration, all while maintaining HIPAA and GCP standards

Qualificações

• Bachelor’s degree in Nursing (or equivalent) with licensure and 4 years in clinical trials coordination or diabetes care.
• Current New York State RN License (as applicable to role).
• Strong communication, organization, and problem-solving abilities.

Responsabilidades

• Manage recruitment, enrollment, and direct care of trial participants.
• Conduct informed consent discussions and coordinate study visits.
• Perform phlebotomy and IV procedures per protocol.
• Administer study medications and educate participants on procedures.
• Document procedures and prepare regulatory submissions for IRB.
• Coordinate with care teams and ensure protocol adherence.

Conhecimentos

Communication skills

Team collaboration

Detail oriented

Multitasking

Microsoft Office

IRB/Good Clinical Practice

Formação académica

Bachelor’s degree in Nursing

Ferramentas

Electronic data capture (EDC)

IRB documentation systems

Descrição da oferta de emprego

The Naomi Berrie Diabetes Center Research Nurse at Columbia University Irving Medical Center coordinates recruitment, enrollment, and direct care for clinical trial participants. You will work with pediatric and adult teams, perform phlebotomy, IV placement, and study drug administration, and ensure protocol adherence.

Responsibilities include consent discussions, scheduling visits, regulatory document preparation, and cross‑functional collaboration, all while maintaining HIPAA and GCP standards