Site Activation Coordinator
IQVIA(20 days ago)
About this role
The Site Activation Coordinator supports and coordinates activation of clinical trial sites from selection through initiation, ensuring efficient, compliant, and timely study start‑up. The role serves as a liaison among sites, internal study teams, sponsors, and regulatory groups to facilitate study start‑up processes.
Required Skills
- Site Activation
- Regulatory Documentation
- CTMS
- IRB Submissions
- Protocol Compliance
- Document Management
- Project Coordination
- Stakeholder Communication
- Metrics Tracking
- ICF Experience
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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