RESEARCH OPERATIONS & REPORTING
Human-subjects research support, scientific project coordination, progress reports, and compliance documentation—from the proposed study through the final report.
Protocol and consent-document preparation, IRB submission support, amendments, and study documentation. Graham Scientific holds FWA00035598; the reviewing IRB and institutional responsibilities are identified for each study.
Translate the work performed into clear accounts of milestones, findings, challenges, changes, and next steps. Support annual, interim, and final sponsor reports, including NIH progress-report preparation within the agreed scope.
Organize applicable requirements, supporting records, reporting obligations, and evidence gaps. Prepare documented status reports and track corrective actions with the responsible research team.
Connect proposal commitments, approved methods, analysis outputs, publications, and reporting milestones. Give investigators and program managers a coherent record across the life of the project.
ONE CONNECTED ENGAGEMENT
A study produces more than a paper. Its scientific and administrative record needs to tell the same story.
We scope the scientific work and its reporting together: named deliverables, responsibility assignments, review points, source records, and submission deadlines. SourceTracer and our private AI workflows support preparation and review; authorized investigators and institutional officials retain their designated approvals.
Contracting & research credentialsLET’S FIND A WAY FORWARD
Start with the scientific aims, current stage, sponsor requirements, and the work your team needs covered.