The role is accountable for delivering global clinical studies within agreed timelines, quality standards, and budgets while ensuring inspection readiness
Job Summary
The role is accountable for delivering global clinical studies within agreed timelines, quality standards, and budgets while ensuring inspection readiness.
Candidates will lead cross-functional teams, manage external vendors, and act as the primary escalation point for resolving study-related issues.
BeOne offers a competitive compensation package including performance-based bonuses, generous equity grants, and opportunities to work with a dynamic global team fighting cancer.
Matching Summary
The role is accountable for delivering global clinical studies within agreed timelines, quality standards, and budgets while ensuring inspection readiness.
Salary
Market competitive compensation; Performance-based annual bonus scheme; Generous welcome grant and performance-based annual equity plan
Skills & Requirements
Must-have
7+ years clinical research experience
Lead global cross-functional study teams
Ensure inspection readiness and GCP compliance
Manage study budgets and vendor invoices
Develop work instructions and SOPs
Nice-to-have
Oncology therapeutic area experience
Biotech or pharma industry background
Collaborative and inclusive team spirit
Experience with complex global studies
Key Requirements
Bachelor's degree in scientific or healthcare discipline
Minimum 7 years of relevant clinical research experience
Proven project management experience in biotech/pharma/CRO
In-depth knowledge of clinical operations methodologies