Research Coordinator - Massachusetts

Job Summary

Detail-oriented and proactive, the full-time Research Coordinator - Evidence Generation in Massachusetts will support clinical and translational research in virally driven cancer diagnostics by coordinating regulatory submissions, managing external research collaborations, and assisting with data management and publication processes.

Key responsibilities

• Coordinate regulatory and IRB submissions, ensuring compliance and maintaining audit-ready documentation across multiple studies
• Serve as the primary point of contact for external collaborators, managing onboarding and tracking collaboration activities
• Collaborate with data scientists to assist in data collection and formatting for statistical analysis, while supporting manuscript development and publication workflows

Required qualifications

• BA/BS or equivalent experience required; MA/MS or MPH in oncology, epidemiology, public health, or a related field strongly preferred
• 3-5 years of experience in clinical research coordination, with a preference for oncology or molecular diagnostics background
• Experience coordinating multi-site or cross-institutional research collaborations
• Familiarity with GCP guidelines, 21 CFR Part 11, and HIPAA requirements as applied to clinical research
• ACRP (CCRC/CCRA), SOCRA (CCRP), or equivalent certification strongly preferred; must obtain GCP certification within 30 days of hire