Clinical Associate Submissions – Regulatory, M.W.D - IQVIA Biotech
IQVIA(1 month ago)
About this role
IQVIA Biotech is hiring a home-based Clinical Associate focused on regulatory submissions in Germany, supporting biotech and emerging biopharma clients. The role operates at a country level with EU CTR requirements for Germany and Austria, acting as a key point of contact across internal teams and investigative sites. The position supports clinical development programs and helps move innovative treatments toward patients faster.
Required Skills
- Regulatory Submissions
- EU CTR
- CTIS
- Site Activation
- Site Start-Up
- Feasibility
- Document Preparation
- Regulatory Compliance
- GCP
- ICH Guidelines
+7 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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