Associate Regulatory & Start Up Manager, IQVIA MedTech Poland
IQVIA(1 month ago)
About this role
Sponsor-facing role responsible for managing site activation, ongoing maintenance, and regulatory activities for selected clinical studies or multi-protocol programs. The position oversees delivery within agreed project scope, timelines, and resources while supporting study initiation and ongoing trial operations across regions.
Required Skills
- Site Activation
- Regulatory Affairs
- Clinical Trials
- Study Start-Up
- Project Management
- Budget Oversight
- Vendor Management
- Stakeholder Management
- Bid Defense
- Regulatory Submissions
+8 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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