With a concentration in the clinical trial and data-based research space, Payal Cramer counsels research institutions, healthcare providers and pharmaceutical and device manufacturers on each aspect of the conduct of human subject research. Her experience includes Food and Drug Administration compliance, Office of Human Research Protections compliance, HIPAA compliance, guidance for research-related Medicare billing, federal grant compliance, contract negotiation and guidance on structuring relationships between institutions, researchers, CROs and sponsors.
