cFSP_SrCRA1_Novartis_Ghana_FSP-2021102842
IQVIA(3 years ago)
About this role
A clinical research role responsible for ensuring study sites conduct trials and report data according to protocol, regulations, and sponsor requirements. The position supports site selection, initiation, monitoring, and close-out activities and maintains regulatory and trial master file documentation. This role is part of IQVIA's clinical research services supporting life sciences clients.
Required Skills
- Site Monitoring
- Site Management
- Recruitment Planning
- Protocol Training
- Regulatory Compliance
- GCP
- ICH
- CRF Management
- TMF Management
- Documentation
+6 more
Qualifications
- High School Diploma Or Equivalent
- Degree In Scientific Discipline Preferred
- 2 Years On-Site Monitoring Experience
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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