Clinical Associate Submissions – Regulatory, Grade 140, M.w.d - Iqvia Biotech

IQVIA UK

Frankfurt, Germany
Eu ctr experience
Local language proficiency
Knowledge of national requirements
IQVIA Biotech partners with biotech and emerging biopharma companies to support clinical development

Job Summary

  • IQVIA Biotech partners with biotech and emerging biopharma companies to support clinical development.
  • You will prepare submission documents and submit to regulatory bodies.
  • You will also ensure adherence to standard operating procedures and project timelines.

Matching Summary

IQVIA Biotech partners with biotech and emerging biopharma companies to support clinical development.

Skills & Requirements

Must-have

  • EU CTR experience
  • local language proficiency
  • knowledge of national requirements

Nice-to-have

  • good negotiating skills
  • effective communication skills
  • mentor junior CSAs

Key Requirements

  • B Sc degree in Health Sciences
  • 1 - 3 years' relevant clinical research experience
  • experience in EUCTR and CTIS submission procedures

Work Rights

Not specified

Tailored Resume

Cover Letter