Clinical Associate Regulatory Submissions - IQVIA Biotech
IQVIA(1 month ago)
About this role
IQVIA Biotech is hiring a Clinical Associate focused on regulatory submissions to support biotech and emerging biopharma companies in clinical development. The role supports assigned studies across Germany and Austria, acting as a key country-level contact for regulatory and start-up activities. It requires local language proficiency, EU CTR/CTIS experience, and familiarity with national submission requirements.
Required Skills
- Regulatory Submissions
- EU CTR
- CTIS
- Site Activation
- Start-Up
- Feasibility
- Site Identification
- Document Review
- Quality Control
- GCP
+5 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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