Provide operational and logistical support to clinical trials in Biomedical Research (BR) with focus on increased complexity and/or priority status
Job Summary
Provide operational and logistical support to clinical trials in Biomedical Research (BR) with focus on increased complexity and/or priority status.
Contribute to the finalization and management of clinical, regulatory and study-related documents in scope of role such as study protocols, patient-facing documents, etc.
Ensure accuracy and completeness of clinical trial management databases, and trial related systems (e.g. Clinical Trial Management System, Novartis Connect).
Matching Summary
Provide operational and logistical support to clinical trials in Biomedical Research (BR) with focus on increased complexity and/or priority status.
Skills & Requirements
Must-have
operational and logistical support
clinical trial lifecycle support
ICH-GCP knowledge
Novartis Standard Operating Procedures
clinical trial management databases
Nice-to-have
process or technology improvements
onboarding and training others
Subject Matter Expert
cross-functional initiatives
Key Requirements
Bachelor’s degree or equivalent qualification or work experience
At least 2+ years’ experience in clinical trial/ development