Senior Study Start up Specialist, IQVIA Biotech
IQVIA(25 days ago)
About this role
A Site Activation specialist at IQVIA coordinates country-level site activation activities for clinical studies, serving as the single point of contact for investigative sites and project teams. The role ensures regulatory compliance, prepares and quality-controls site documents, maintains tracking systems, and provides local expertise to meet project timelines and contractual requirements.
Required Skills
- Site Activation
- Regulatory Documentation
- Project Management
- Quality Control
- GCP/ICH
- Communication
- Stakeholder Management
- Document Tracking
Qualifications
- Bachelor's Degree in Life Sciences or Related Field
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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