Regulatory and Start Up Specialist
IQVIA(2 months ago)
About this role
This role supports country-level site activation for clinical studies, ensuring startup documentation and approvals progress smoothly in line with project requirements and regulatory expectations. The position serves as a key coordination hub between investigative sites and internal study teams while providing local expertise for Norway. It is a home-based role requiring fluency in Norwegian.
Required Skills
- Site Activation
- Study Start-Up
- Regulatory Documents
- GCP
- ICH
- Clinical Systems
- SOP Compliance
- Timeline Planning
- Document Tracking
- Quality Control
+2 more
Qualifications
- Bachelor’s Degree In Life Sciences
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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