Clinical Research Associate, Sponsor Dedicated, Oncology or Immunology
IQVIA(27 days ago)
About this role
The Clinical Research Site Manager oversees the operation and regulatory compliance of clinical study sites, ensuring adherence to protocols, sponsor requirements, and applicable guidelines. The role supports study execution across start-up, monitoring, and close-out phases while coordinating with study teams and site staff. The position involves regular travel to sites to maintain oversight and site relationships.
Required Skills
- Site Monitoring
- Recruitment Management
- Protocol Training
- Quality Assurance
- Regulatory Tracking
- TMF Management
- CRF Completion
- Data Queries
- Mentorship
- Microsoft Excel
+6 more
Qualifications
- BS Degree in Scientific Discipline
About IQVIA
iqvia.comIQVIA is a leading global provider of data, technology, and advanced analytics focused on transforming healthcare and life sciences. The company empowers organizations to accelerate innovation, enhance patient outcomes, and expedite the market introduction of new treatments through comprehensive healthcare analytics and real-world evidence. With a commitment to Human Data Science, IQVIA combines its extensive expertise with innovative technology to improve health outcomes worldwide.
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