Germany onlyClinical Associate Submissions – Regulatory role at IQVIA Biotech, supporting clinical development in biotech and emerging biopharma companies in Germany and Austria.
Requirements
- B Sc degree in Health Sciences or related field
- 1-3 years' relevant clinical research experience, specifically in submissions
- Experience in EUCTR and CTIS submission procedures
- Good negotiating and communication skills in local language
- Effective communication, organizational, and interpersonal skills
- Ability to work independently and to effectively prioritize tasks
- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
Benefits
- IQVIA is a leading global provider of clinical research services
- Collaborative culture, and deep therapeutic expertise
- Support clinical development across all phases and therapeutic areas
United States only
Australia only