Oncology Clinical Data Coordinator

NYU Langone Hospitals; New York (NY); On-site; USD 48,000 - 59,000; Full time

Job summary

NYU Langone Health is seeking a Research Data Associate to coordinate basic level cancer clinical research studies at the Laura and Isaac Perlmutter Cancer Center. You will perform enrollment and data entry, interfacing with investigators and study teams under supervision.

The role involves data coordination, regulatory tasks, and collaboration with radiology, pathology, and research support staff to ensure timely, accurate study documentation and compliance with GCP guidelines.

Qualifications

• Associate's degree plus one year related experience or equivalent combination.
• Bachelor's degree preferred.
• Computer literate with good interpersonal, writing and verbal communication skills.

Responsibilities

• Data entry for cancer clinical studies and enrollment within 1 week or less from last visit.
• Log visits into CRMS to ensure timely billing for research procedures.
• Request pathology reports and tissue acquisition per protocol.
• Coordinate imaging submissions with the Department of Radiology.
• Schedule monitoring visits and coordinate with monitors and staff; manage charts and access.
• Perform vial assignments and assist with eligibility review and subject registration.
• Coordinate SAE submissions to DSMC, sponsor, and IRB.
• Develop understanding of GCP and related regulatory policies.
• Collect patient information and abstract data for publications; maintain data quality and accuracy.
• Attend research meetings and report progress to sponsors.

Skills

Interpersonal communication

Writing skills

Verbal communication

Computer literacy

Education

Associate's degree

Bachelor's degree

Tools

CRMS (Clinical Research Management System)

EMR (Electronic Medical Records)

Job description

NYU Langone Health is seeking a Research Data Associate to coordinate basic level cancer clinical research studies at the Laura and Isaac Perlmutter Cancer Center. You will perform enrollment and data entry, interfacing with investigators and study teams under supervision.

The role involves data coordination, regulatory tasks, and collaboration with radiology, pathology, and research support staff to ensure timely, accurate study documentation and compliance with GCP guidelines.