Site Activation Specialist
IQVIA(1 month ago)
About this role
This role supports the regulatory start-up and ongoing maintenance of clinical studies, serving as the primary point of contact between investigative sites and internal project stakeholders. It focuses on enabling sites to be ready to initiate and conduct clinical trial activities through coordinated documentation, approvals, and operational alignment. The position operates within a regulated clinical trial environment at IQVIA, a global clinical research services provider to the life sciences and healthcare industries.
Required Skills
- Clinical Start-Up
- Regulatory Submissions
- Site Contracts
- Budget Negotiation
- Site Management
- Project Timelines
- SOP Compliance
- Clinical Systems
- GCP
- ICH Guidelines
+5 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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