- IQVIA (Durham, NC)
- …manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award ... resolving project related issues where required. Ensure collaboration across Regulatory & Site Activation, including communication with regions and countries,… more
- IQVIA (Durham, NC)
- …activities that may include: . Site identification and feasibility activities, Regulatory , start -up, and maintenance activities . Preparation, review, ... negotiation and management of site regulatory documentation and clinical trial agreements with sites and sponsors . Maintains, reviews, and reports on site… more
- ThermoFisher Scientific (Las Vegas, NV)
- …PPD(R) clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and ... process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from… more
- ThermoFisher Scientific (Columbus, OH)
- …PPD(R) clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and ... process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from… more