Clinical Research Coordinator – Trials & Data Mgmt

danafarber; Boston (MA); On-site; USD 52,000 - 78,000; Full time

Job summary

Dana-Farber Cancer Institute in Boston is seeking a Clinical Research Coordinator to support the research team in conducting clinical trials under Good Clinical Practice guidelines. You will manage data collection and packet integrity, participate in protocol assessments, and maintain trial binders to ensure regulatory compliance.

Responsibilities include coordinating regulatory submissions, obtaining informed consent when required, and facilitating data entry into the Clinical Trial Management

Qualifications

• Bachelor's Degree or 1 year Dana‑Farber Associate Clinical Research Coordinator experience.
• 0-1 years of experience working in a medical or scientific research setting preferred.

Responsibilities

• Collect, manage, and report patient data for clinical trials.
• Support protocol assessments and IRB submissions as required.
• Maintain study and regulatory binders to ensure compliance with state, federal, and IRB requirements.
• Screen patients for protocol eligibility and obtain informed consent where applicable.
• Coordinate data entry into the Clinical Trial Management System (ONCORE) and communicate with sponsors.

Skills

Organizational skills

Interpersonal skills

Attention to detail

Time management

Discretion

MS Office

Education

Bachelor's Degree

Tools

ONCORE

Job description

Dana-Farber Cancer Institute in Boston is seeking a Clinical Research Coordinator to support the research team in conducting clinical trials under Good Clinical Practice guidelines. You will manage data collection and packet integrity, participate in protocol assessments, and maintain trial binders to ensure regulatory compliance.

Responsibilities include coordinating regulatory submissions, obtaining informed consent when required, and facilitating data entry into the Clinical Trial Management