Clinical Trials Research Associate — Data & Coordination

Montefiore Hudson Valley Collaborative; New York (NY); On-site; USD 56,000 - 70,000; Full time

Job summary

The Montefiore Hudson Valley Collaborative is seeking a Research Associate to support the Cancer Clinical Trials Office's solid tumor program. Under supervision, you will collect and manage patient data and assist with consent and sample handling in interventional and non-interventional studies.

You will participate in screening, data entry into our databases, and coordinating scheduling and shipments, ensuring source documents are complete and compliant with Good Clinical Practice.

Qualifications

• Bachelor's degree in life science or public health required.
• Master's degree preferred; related advanced degrees welcomed.
• ACRP or SOCRA certification preferred.

Responsibilities

• Collects and records study data; inputs information into database.
• Assists in activities related to clinical research studies, including screening participants.
• Maintains source documents and subject files per hospital procedures.
• Coordinates scheduling and monitoring visits, including remote access setup.
• Secures, delivers and ships clinical specimens as required by protocol.
• Supports informed consent processes for interventional and non-interventional trials.

Skills

Data collection

Good Clinical Practice

Informed consent

Clinical trial coordination

Education

Bachelor's degree in life science or public health

Master's degree preferred

Medical Degree (or foreign equivalent), preferred

Tools

ACRP/SOCRA certification

Job description

The Montefiore Hudson Valley Collaborative is seeking a Research Associate to support the Cancer Clinical Trials Office's solid tumor program. Under supervision, you will collect and manage patient data and assist with consent and sample handling in interventional and non-interventional studies.

You will participate in screening, data entry into our databases, and coordinating scheduling and shipments, ensuring source documents are complete and compliant with Good Clinical Practice.