Regulatory & Start-Up Specialist 2, IQVIA Biotech, Nordic Regions
IQVIA(2 months ago)
About this role
This homebased role supports clinical trial regulatory submissions and site activation activities for studies in Sweden, Norway, or Denmark. It serves as a key country-level contact for investigative sites and internal stakeholders, ensuring local regulatory alignment and timely study start-up progress. The position requires Nordic local language proficiency and hands-on EU CTR/CTIS experience.
Required Skills
- Regulatory Submissions
- Site Activation
- EU CTR
- CTIS
- Feasibility
- Start-Up
- Document Review
- Ethics Submissions
- Informed Consent
- Site Contracts
+8 more
Qualifications
- BSc In Health 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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