Clinical Research Associate — Cancer Trials & Data

Montefiore; New York (NY); On-site; USD 55,000 - 75,000; Full time

Job summary

Montefiore is seeking a Cancer Clinical Trials CRC I to support the research team in the conduct of clinical trials under Good Clinical Practice. This role focuses on primary data collection and management of patient information for interventional and non-interventional studies, guided by a senior coordinator.

Responsibilities include obtaining informed consent, assisting recruitment, recording data in the database, maintaining source documents, and coordinating scheduling and specimen handling

Qualifications

• Bachelor's Degree required for CRC I position.
• Master's Degree preferred to support clinical trials.
• ACRP or SOCRA certification preferred for credentials.
• Bachelor's in life science or public health preferred.
• Medical degree or foreign equivalent preferred.

Responsibilities

• Collects and records study data; inputs into database.
• Assists in activities related to clinical studies, including screening participants and registering subjects.
• Maintains source documents and subject files per hospital procedures.
• Ensures accurate compilation of subject data through chart reviews.
• 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 knowledge

Good Clinical Practice (GCP)

Informed consent

Study coordination

Education

Bachelor's Degree Required

Master's Degree Preferred

ACRP/SOCRA certification preferred

Bachelor's in life science or public health preferred

Medical Degree or foreign equivalent, Preferred

Job description

Montefiore is seeking a Cancer Clinical Trials CRC I to support the research team in the conduct of clinical trials under Good Clinical Practice. This role focuses on primary data collection and management of patient information for interventional and non-interventional studies, guided by a senior coordinator.

Responsibilities include obtaining informed consent, assisting recruitment, recording data in the database, maintaining source documents, and coordinating scheduling and specimen handling