The role involves building and influencing a broad cross-functional study level network to ensure quality, efficiency, and patient-centric approaches
Job Summary
The role involves building and influencing a broad cross-functional study level network to ensure quality, efficiency, and patient-centric approaches.
Candidates will be accountable for developing essential study documents like Clinical Study Protocols and Reports while ensuring data accuracy and timeliness.
Roche offers a culture that encourages personal expression, open dialogue, and genuine connections where every voice matters.
Matching Summary
The role involves building and influencing a broad cross-functional study level network to ensure quality, efficiency, and patient-centric approaches.
Skills & Requirements
Must-have
Lead cross-functional study teams
Manage clinical study budgets
Ensure ICH-GCP compliance
Oversee CRO partnerships
Develop Clinical Study Protocols
Nice-to-have
Drive innovation in operations
Patient-centric approach
Health equity research commitments
Strategic critical thinking abilities
High performing organization mindset
Key Requirements
Minimum 7 years clinical R&D experience
2 years project management experience
University degree in medical or biological sciences