Study Start-Up Specialist 1, IQVIA Biotech, Poland
IQVIA(1 month ago)
About this role
A Study Start-Up Specialist at IQVIA Biotech supports biotech clinical development by coordinating country-level start-up and regulatory activities to enable timely site activation. The role works with project teams and investigative sites to ensure compliance with applicable local and international regulations and corporate standards. This is a homebased position based in Poland within IQVIA’s biotech delivery model.
Required Skills
- Site Activation
- Feasibility
- Regulatory Submissions
- EDP Compilation
- Document Review
- Project Management
- Clinical Systems
- GCP/ICH
- Communication
- Negotiation
+1 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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