Clinical Research Coordinator - Breast Oncology

About the role

The CRC works within the Breast Oncology clinical research program and supports the research team in conducting clinical trials under Good Clinical Practice. Responsibilities include primary data collection and management, ensuring timely trial assessments and sample collection, maintaining participant binders, and supporting IRB protocol submissions.

Responsibilities

• Primary data collection and management of patient clinical information
• Timely facilitation of trial assessments and collection of protocol-related samples
• Maintain and organize study participant/subject trial binders and regulatory binders
• Support and maintain participant/subject trial binders and may maintain regulatory binders
• Screen patients for protocol eligibility, obtain informed consent for non-treatment trials, and register study participants with the clinical trials management system
• Prepare and/or complete regulatory related reports and IRB submissions
• Organize and prepare for both internal and external auditing and study monitoring visits
• Coordinate and manage clinical trials throughout their lifecycle, including communication with sponsors and regulatory authorities
• Close out clinical trials, contributing to research articles, audit preparation, and communication with regulatory agencies and other disciplines involved
• Interact with study participants as directed/required by the protocol and/or study team
• May be responsible for tissue sample collection per trial requirements
• Data entry of Subject Visit Tracking information into Clinical Trial Management System
• Data entry of time and effort spent on study-specific activities and other administrative tasks into Clinical Trial Management System
• Data entry of study-specific activity, including but not limited to monitor visits, external site enrollment, amendments, receipt of Safety Reports, etc. into Clinical Trial Management System

Requirements

• Bachelor’s Degree or 1 year of Dana-Farber Associate Clinical Research Coordinator experience required
• 0-1 years of experience working in a medical or scientific research setting or comparable technology orientated business environment preferred

Qualifications

• Excellent organization and communications skills required
• Strong interpersonal skills – ability to effectively interact with all levels of staff and external contacts
• Detail-oriented and able to follow-through
• Ability to effectively manage time and prioritize workload
• Practice discretion and adhere to hospital confidentiality guidelines at all times
• Computer skills including the use of Microsoft Office

Skills

• Knowledge of Good Clinical Practice (GCP)
• Experience with clinical trial management systems
• Ability to manage multiple projects simultaneously
• Strong attention to detail
• Effective communication and interpersonal skills

Benefits

Located in Boston and the surrounding communities, Dana-Farber Cancer Institute offers a supportive and inclusive environment. The institute provides comprehensive care to patients of all backgrounds and designs programs to promote public health, particularly among high-risk and underserved populations.

Pay

$48,100.00 - $54,400.00

Schedule

N/A