My multinational pharmaceutical client is currently looking for a Clinical Trials Capabilities Associate (Any European Language) to join their expanding team based in Cork.
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.
This is an exciting opportunity 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 & any European Language
Please contact TJ on 021 235 9144 or email@example.com for a confidential discussion
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