Cancer Trials Research Data Associate

3000 Montefiore Medical Center; New York (NY); On-site; USD 56,000 - 70,000; Full time

Benefits offered by this job

Insurance benefits

Comprehensive benefits

Job summary

Montefiore Medical Center in Bronx, NY, is hiring a CRC I for the Cancer Clinical Trials Office–Operations-Solid Tumors. The role supports the research team in data collection, consent processes, and coordinating study activities under supervision.

Under supervision, you will input data, assist with recruitment, and manage study documents to ensure compliance with protocols and sponsor requirements. Day shift, M-F, 9 AM–5:30 PM.

Qualifications

• Bachelor’s degree required.
• Master’s degree preferred.
• Bachelor’s degree in life science or public health preferred.
• Medical Degree (or foreign equivalent) preferred.

Responsibilities

• Collects and records study data.
• Inputs all information into database.
• Assists in activities related to clinical research studies including but not limited to answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.
• Maintains source documents and subject files in accordance with hospital procedures.
• Coordinates SFV, SIVs and monitor scheduling-- including remote access setup--for multiple studies.
• Secures, delivers and ships clinical specimens as required by the protocol.

Skills

Data collection

Clinical research

Good Clinical Practice

Education

Bachelor’s degree required

Master’s degree preferred

Life science/public health background preferred

Medical degree (or foreign equivalent)

Job description

Montefiore Medical Center in Bronx, NY, is hiring a CRC I for the Cancer Clinical Trials Office–Operations-Solid Tumors. The role supports the research team in data collection, consent processes, and coordinating study activities under supervision.

Under supervision, you will input data, assist with recruitment, and manage study documents to ensure compliance with protocols and sponsor requirements. Day shift, M-F, 9 AM–5:30 PM.