Practicante Regulatorio De Global Clinical Trial Operations

med-in.at

Hybrid
Regulatory document preparation
Clinical trial submissions
Document review and editing
The position is an internship opportunity at med-in.at within the Global Clinical Trial Operations division, focusing on regulatory affairs related to clinical trials. Ideal candidates are pharmacy or biochemistry students with intermediate English proficiency and strong analytical skills

Job Summary

  • Our Regulatory Affairs team brings new medical advancements to the world by facilitating communications and procedures that enable rapid and organized compliance with external regulatory agencies.
  • The position's objectives include providing administrative support in the preparation of submissions to regulatory authorities and monitoring submitted files.
  • The role involves reviewing standard documents, editing informed consent forms, and supporting the submission of safety reports to Ethics Committees.

Matching Summary

Match Score: 85

The position is an internship opportunity at med-in.at within the Global Clinical Trial Operations division, focusing on regulatory affairs related to clinical trials. Ideal candidates are pharmacy or biochemistry students with intermediate English proficiency and strong analytical skills.

Skills & Requirements

Must-have

  • Regulatory document preparation
  • Clinical trial submissions
  • Document review and editing
  • Regulatory compliance monitoring
  • Internal stakeholder coordination

Nice-to-have

  • Proactive process improvement
  • Cross-functional collaboration
  • Patient-first ideology

Key Requirements

  • University students in Pharmacy and/or Biochemistry
  • Intermediate English level

Work Rights

Not specified

Tailored Resume

Cover Letter