At Roche you can show up as yourself, embraced for the unique qualities you bring
Job Summary
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Lead and coordinate a cross-functional study team of experts, in compliance with ICH-GCP and Roche processes in accordance SOPs and guidelines to ensure the clinical study progresses as planned.
Develop and oversee the study budget throughout the study lifecycle including budget re-forecasting, identification of any financial risks and enactment of mitigation plans.
Matching Summary
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Skills & Requirements
Must-have
ICH-GCP compliance
Clinical study document development
Quality risk strategy
Cross-functional team leadership
External service provider oversight
Study budget management
Nice-to-have
Personal expression encouraged
Open dialogue and genuine connections
Patient and investigator-centric approach
Innovation in clinical operations
Key Requirements
University degree in medical or biological sciences
Minimum 7 years clinical experience in R&D
2 years project management experience
Extensive knowledge of clinical research regulatory requirements