Regulatory and Site Activation Sr Analyst
IQVIA(1 month ago)
About this role
This role supports country/region-level site activation for clinical studies, ensuring documentation and processes align with local/international regulations, SOPs, and project guidelines. The position works closely with project and site activation stakeholders to help move investigative sites through activation and related start-up activities within IQVIA’s clinical research operations.
Required Skills
- Site Activation
- Feasibility
- Regulatory Submissions
- Document Review
- Clinical Trials
- Ethics Review
- Informed Consent
- Investigator Pack
- Contract Management
- Database Updates
+3 more
Qualifications
- Bachelor's Degree In Life Science 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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