My multinational pharmaceutical client is currently recruiting for a German Clinical Trials Associate to join their expanding team.
Your role would be to provide excellent and efficient support of clinical development by enrolling study participants, obtaining clinical trial authorisations, ethical approvals and record management.
Ideally this role would suit someone who demonstrates understanding of overall clinical development paradigm and experience working in a compliance-driven environment.
Day to day responsibilities would include but not limited to:
- Ensure inspection readiness through a complete, accurate and readily available Trial Master File
- Collection and submission of regulatory documents, customization and negotiation of informed consent documents, serve as the point of contact
- Ensure country specific regulatory and data privacy requirements are incorporated into submission documents and any other documents/systems
- Understand and comply with procurements, legal and financial requirements and procedures
- Populate Trial Master Files and libraries for future reference
- Bachelor’s degree in scientific or health field
- Minimum 2 years clinical research or relevant experience preferred
- Fluency in English & German language
Please contact Marie on 021 484 7133 or firstname.lastname@example.org for a confidential discussion
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