Full-time · On-site

Clinical Research Coordinator

This is a premier entry-level opportunity for a graduating senior to enter the clinical research field at one of the world's top cancer institutes. The role balances administrative rigor with patient-facing responsibilities, providing a 360-degree view of how medical breakthroughs are validated. It is an ideal stepping stone for those looking to build a career in medicine, public health, or biotechnology.

DC
Hiring company

Dana-Farber Cancer Institute

Boston, Massachusetts, United States · Posted 29 April 2026

The role

Overview

This is a premier entry-level opportunity for a graduating senior to enter the clinical research field at one of the world's top cancer institutes. The role balances administrative rigor with patient-facing responsibilities, providing a 360-degree view of how medical breakthroughs are validated. It is an ideal stepping stone for those looking to build a career in medicine, public health, or biotechnology.

The hiring side

About Dana-Farber Cancer Institute

Dana-Farber Cancer Institute is a large employer working in healthcare and biotechnology, based in Boston, Massachusetts, United States.

Industry

Healthcare and Biotechnology

Size

Large

Location

Boston, Massachusetts, United States

Go deeper

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Research Dana-Farber Cancer Institute

What they need

Requirements & Skills

Key Responsibilities

  • Overseeing the start-up process for clinical trials from protocol receipt to site activation
  • Managing data reporting, source document collection, and resolution of data queries
  • Preparing and submitting regulatory reports to the Institutional Review Board (IRB)
  • Ensuring biological samples are prepared and shipped according to strict safety regulations
  • Organizing site visits for internal monitoring and external auditing bodies

Essential

  • Adherence to Good Clinical Practice (GCP) standards
  • Ability to manage primary data collection and patient clinical information
  • Capacity to facilitate trial assessments and collect/ship protocol samples
  • Maintenance of participant trial binders and regulatory documentation
  • Willingness to travel as required for study needs
  • Ability to coordinate with multidisciplinary teams including Pharmacy and Nursing

Preferred

  • Experience with IRB protocol submissions
  • Familiarity with the ONCORE clinical trials management system
  • Interest in contributing to research articles and publications
  • Experience with internal and external auditing preparation

Key Skills

Data management and reportingRegulatory compliancePatient screening and informed consentIATA/DOT regulation knowledge for sample shippingOrganizational and archiving skillsInterdisciplinary collaboration

Networking

People to Know

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Perks

Benefits & perks

  • Opportunity to work at a Harvard Medical School-affiliated hospital
  • Exposure to groundbreaking cancer research and treatment breakthroughs
  • Inclusive and diverse work environment
  • Professional development in clinical trial management
  • Collaborative culture with world-class medical partners

Next step

Apply now

Found via careerservices.fas.harvard.edu

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