Regulatory and Start Up Specialist - Greece
IQVIA(1 month ago)
About this role
This role supports country-level clinical trial site activation activities to help initiate and maintain investigative sites in line with project requirements and regulatory expectations. The position acts as a key coordination point between investigative sites and internal study teams to enable timely study start-up. It is a hybrid role requiring Greek language fluency and in-office presence once per week.
Required Skills
- Site Activation
- Clinical Research
- Regulatory Documents
- GCP
- ICH
- SOP Compliance
- Project Timelines
- Document Tracking
- Database Maintenance
- Quality Control
+3 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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