- IQVIA (Durham, NC)
- …training and experience. * In-depth knowledge of applicable clinical research regulatory requirements (ie, Good Clinical Practice (GCP) and International Conference ... on Harmonization (ICH) guidelines). * Good leadership skills. * Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint. * Written and verbal communication skills including good command of English. * Excellent organizational and… more
- ThermoFisher Scientific (Greenville, NC)
- …timely deliverables, monitors trials, communicates with study sites, coordinates start -up activities, addresses regulatory requirements and provides input ... meetings with Sponsor to discuss, but not limited to country/region start up progress, trending and issue identification/escalation, and general site/country… more
- ThermoFisher Scientific (Greenville, NC)
- …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 ... minimize delays, and execute high-quality, cost-efficient clinical studies. The PPD FSP Solution: PPD's Functional Service Provider division partner with and serve… more
- Bristol Myers Squibb (Madison, NJ)
- …types (eCRF and non eCRF) collected in BMS clinical trials from study start to database lock. **Position Summary** The Senior Manager, Clinical Data Management is ... and audits + Provides coaching and quality oversight of junior Data Management Leads ** FSP /CRO/Vendor Oversight** + May act as core member of the study team and… more