Clinical Research Associate - Sponsor dedicated
IQVIA(4 years ago)
About this role
A Clinical Research Site Monitor at IQVIA is a mid-level clinical trials professional within the contract research organization supporting life sciences clients. The role focuses on ensuring clinical studies are conducted in accordance with protocols, regulatory requirements, and sponsor expectations while interacting with investigator sites and internal study teams.
Required Skills
- Site Monitoring
- Patient Recruitment
- Protocol Training
- Regulatory Compliance
- GCP
- ICH
- CRF Management
- TMF Management
- Documentation
- Communication
+2 more
Qualifications
- High School Diploma
- Degree In Scientific Discipline (Preferred)
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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