
Dartmouth-Hitchcock Research Administration provides dedicated space and staff for the efficient conduct of clinical research across the life cycle of a project. Research nurses and coordinators assist with study preparation, regulatory and IRB submissions, study procedures and sample processing according to protocol requirements.
Learn MoreDartmouth-Hitchcock Clinical Trials Office (CTO) supports initiation and conduct of high-quality clinical studies through investigator collaboration, contract/budget/MCA review, and regulatory support for GCP compliance.
Learn MoreConnects local researchers with an extensive NCATS national network offering comprehensive research development services and opportunities to lead or collaborate on multi-site clinical trials.
Provides Dartmouth investigators with: • CTSA consultation and resources to develop high-impact clinical research protocols • Opportunities to participate in multi-center clinical trials
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