Clinical Research Coordinator — Trials & Data Management

danafarber; Boston (MA); On-site; USD 65,000 - 95,000; Full time

Job summary

The Dana-Farber Cancer Institute in Boston is seeking a Clinical Research Coordinator to support the conduct of clinical trials under Good Clinical Practice (GCP). The role focuses on data collection, management of source documents, CRFs, adverse events reporting, and ensuring regulatory compliance across trial activities.

Responsibilities include screening patients for eligibility, obtaining informed consent for non-treatment trials, registering participants in ONCORE, maintaining trial and

Qualifications

• Bachelor's degree is required or equivalent Dana‑Farber CRC experience.
• Experience in clinical trial data collection and regulatory binder maintenance preferred.
• Experience with regulatory submissions and IRB processes is an asset.

Responsibilities

• Coordinate data collection and management of patient clinical information.
• Facilitate trial assessments per protocol and ship samples as required.
• Maintain participant trial binders and regulatory binders to ensure compliance.
• Assist with IRB submissions and protocol submissions.
• Screen patients for eligibility and obtain informed consent for non-treatment trials.
• Register study participants in the ONCORE system.
• Support trial start-up, monitoring visits, and audits.
• Collaborate with Protocol Scheduling, Materials Management, labs, nursing, and other departments.
• Travel may be required.

Skills

Excellent organization

Strong interpersonal skills

Attention to detail

Time management

Discretion and confidentiality

MS Office proficiency

Education

Bachelor's degree

Tools

Microsoft Office

Job description

The Dana-Farber Cancer Institute in Boston is seeking a Clinical Research Coordinator to support the conduct of clinical trials under Good Clinical Practice (GCP). The role focuses on data collection, management of source documents, CRFs, adverse events reporting, and ensuring regulatory compliance across trial activities.

Responsibilities include screening patients for eligibility, obtaining informed consent for non-treatment trials, registering participants in ONCORE, maintaining trial and