Clinical Research Coordinator - Breast Oncology Cohort Studies Program

Center for Patient Derived Models - Dana-Farber Cancer Institute; Boston (MA); On-site; USD 45,000 - 70,000; Full time

Job summary

An established industry player is seeking a Clinical Research Coordinator for its Breast Oncology Cohort Studies Program. This role involves supporting clinical and translational research through patient screening, data collection, and collaboration with investigators. As part of a leading cancer research institute, you will contribute to groundbreaking studies while ensuring data integrity and regulatory compliance. This position is perfect for recent graduates eager to make an impact in the medical research field and work in a diverse, inclusive environment.

Qualifications

• Bachelor's degree required; 0-1 years of related experience preferred.
• Experience in medical or scientific research preferred.

Responsibilities

• Screen patients for protocol eligibility and obtain informed consent.
• Review and abstract clinical information from medical records.
• Collaborate with research staff on translational studies.

Skills

Organization Skills

Communication Skills

Interpersonal Skills

Detail-oriented

Time Management

Microsoft Office Proficiency

Education

Bachelor's Degree

Job description

Clinical Research Coordinator - Breast Oncology Cohort Studies Program

Join to apply for the Clinical Research Coordinator - Breast Oncology Cohort Studies Program role at Center for Patient Derived Models - Dana-Farber Cancer Institute.

Location: 450 Brookline Ave, Boston, MA 02215

Category: Clinical Research

Employment Type: Full time

Work Location: Onsite: 4-5 days onsite/week

Overview

The Clinical Research Coordinator will support the Breast Oncology Cohort Studies Program and its clinical and translational research, including screening, recruitment, data collection, biospecimen collection, and database organization. Responsibilities include reviewing medical records, collecting biospecimens, and assisting with patient screening, consent, and registration. The position may also involve collaboration with investigators and external partners, data management, and regulatory tasks.

We are considering 2025 bachelor's degree graduates for this position.

Located in Boston, Dana-Farber Cancer Institute is a leader in cancer research and patient care, committed to diversity, equity, and inclusion, and advancing treatment through groundbreaking research.

Responsibilities

• Screen patients for protocol eligibility, obtain informed consent, and register study participants.
• Interact with study participants as directed.
• Review and abstract clinical information from medical records.
• Verify data quality and completeness.
• Collaborate with research staff and external partners on translational studies.
• Assist in creating lists of patients and samples for study management.
• Support the collection and labeling of biological specimens and regulatory documentation.

Qualifications

• Bachelor's Degree required; 0-1 years of related experience preferred.
• Experience in medical or scientific research or similar environment preferred.

Knowledge, Skills, and Abilities

• Excellent organization and communication skills.
• Strong interpersonal skills.
• Detail-oriented with good follow-through.
• Effective time management and prioritization.
• Discretion and confidentiality adherence.
• Proficiency in Microsoft Office.

We are committed to creating an inclusive environment and encourage diverse applicants to apply.