PI & site medical directorship
Clinical leadership, medical decisions, eligibility, participant safety and oversight of delegated activities.
Site partners
PI and Site Research Medical Director support for established sites and site networks: medical oversight, feasibility review, study preparation and sponsor/CRO engagement.
Strengthen your site’s presentation to sponsors and CROs with a qualified investigator whose clinical background and research experience match the protocol.
Clinical leadership, medical decisions, eligibility, participant safety and oversight of delegated activities.
Medical review of protocols, study populations, resources, facilities and site readiness before study acceptance.
Oversight of credential review, protocol-specific training and staff suitability for delegated responsibilities.
Physician participation in feasibility, site-selection and study meetings, with review and escalation of clinical concerns.
Represent your site at clinical research events nationwide, with agreed messaging and partnership objectives.
Engagement process
Dr. Falcon leads physician investigator services. Each proposed investigator is reviewed for credentials, relevant experience, location and availability. Primary and backup coverage are defined for the study before acceptance.
Appointments require a qualified site, adequate resources, applicable approvals and separate written acceptance. Readiness consulting is optional and does not influence appointment. The PI retains oversight of delegated activities.