Clinical Trials Data & Compliance Coordinator

Dana-Farber Cancer Institute; Brookline, Northern (MA, KY); Hybrid; USD 48,000 - 54,000; Full time

Job summary

Dana-Farber Cancer Institute seeks a Clinical Research Coordinator to support trial conduct under GCP. You will collect and manage patient data, facilitate assessments, and ensure compliance with IRB requirements and study protocols. Collaboration with multiple departments and potential travel are involved.

The role emphasizes meticulous data entry, binder maintenance, and regulatory support to uphold trial integrity and patient safety. A Bachelor’s Degree and CRC experience are preferred.

Qualifications

• Bachelor’s degree or equivalent experience in a clinical or scientific setting.
• 0–1 years of Dana-Farber Associate Clinical Research Coordinator experience preferred.
• Experience in medical or scientific research environment preferred.

Responsibilities

• Oversee data collection and management of patient clinical information for trials.
• Facilitate trial assessments per protocol and collect samples per requirements.
• Maintain study and regulatory binders and ensure IRB compliance as needed.
• Enter data into the Clinical Trials Management System and support source documents.
• Coordinate with internal teams and external sites; assist with audits and monitoring.

Skills

Organization

Communication

Detail oriented

Time management

Discretion

Education

Bachelor’s Degree

Tools

Microsoft Office

Job description

Dana-Farber Cancer Institute seeks a Clinical Research Coordinator to support trial conduct under GCP. You will collect and manage patient data, facilitate assessments, and ensure compliance with IRB requirements and study protocols. Collaboration with multiple departments and potential travel are involved.

The role emphasizes meticulous data entry, binder maintenance, and regulatory support to uphold trial integrity and patient safety. A Bachelor’s Degree and CRC experience are preferred.