Breast Oncology Clinical Trials Coordinator

Dana-Farber Cancer Institute, Inc.; Boston (MA); On-site; USD 48,000 - 54,000; Full time

Job summary

Dana-Farber Cancer Institute in Boston seeks a Clinical Research Coordinator to support breast oncology trials under GCP. You will manage data collection, regulatory binders, informed consent, and ONCORE registrations, ensuring timely trial assessments and protocol compliance. Some travel may be required.

Located in Boston, Dana-Farber leads in cancer research and patient care, fostering diversity, inclusion, and high-quality clinical data across trials.

Qualifications

• Bachelor’s Degree or equivalent experience in clinical research.
• Proven ability to manage study data and regulatory documents.
• Familiarity with clinical trial workflows and IRB submissions.

Responsibilities

• Oversight of start-up processes, IRB submissions, and site activations.
• Data reporting, collection of source documents, case report forms, and queries.
• Maintain study binders and regulatory binders; ensure protocol compliance.
• Coordinate sample collection, preparation, and shipping per protocol.
• Prepare regulatory reports and inputs for audits and monitoring visits.
• Interact with sponsors, regulatory authorities, and study team.

Skills

Excellent organization

Strong interpersonal skills

Attention to detail

Time management

Discretion

Microsoft Office

Education

Bachelor’s Degree

Dana-Farber Associate CRC experience

Tools

ONCORE

Job description

Dana-Farber Cancer Institute in Boston seeks a Clinical Research Coordinator to support breast oncology trials under GCP. You will manage data collection, regulatory binders, informed consent, and ONCORE registrations, ensuring timely trial assessments and protocol compliance. Some travel may be required.

Located in Boston, Dana-Farber leads in cancer research and patient care, fostering diversity, inclusion, and high-quality clinical data across trials.