- 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
- AbbVie (North Chicago, IL)
- …the validation of electronic systems, software & programs applied internally per current regulatory requirements such as 21 CFR Part 11 & ICH- GCP. + Provide ... data capture, review and database lock activities for programming activities from start -up through statistical analysis stage of clinical studies. + Lead the… 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