Senior Director, Clinical Operations & Study Delivery

BioSpace

South San Francisco (CA)

On-site

USD 232,000 - 283,000

Full time

14 days+
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Benefits offered by this job

Annual bonus
Equity incentive plan
401(k) match
Medical, dental & vision insurance

Job summary

Maze Therapeutics in South San Francisco seeks an Oversight Director, Clinical Operations to provide strategic and operational leadership across CKD and PKU programs from early development through pivotal studies. You will shape development strategy, oversee CRO/vendor relationships, and ensure high-quality trials on time and budget.

You will guide Study Leads and build a high-performing Clinical Operations team, driving risk management, resource planning, and regulatory readiness to support

Qualifications

  • Bachelor’s degree in a scientific or health-related field; 12–15+ years in clinical operations
  • Experience leading global Phase I–III trials and overseeing development assets
  • Proven ability to guide and develop Clinical Operations teams and study leads
  • Deep expertise in FDA/EMA/ICH-GCP regulatory requirements and inspection readiness

Responsibilities

  • Provide strategic and operational direction across multiple studies within the asset
  • Oversee CRO and vendor strategies, budgets, and master service agreements
  • Lead resource planning, forecasting, and budget accountability for Clinical Operations
  • Ensure inspection readiness and compliance with SOPs and regulatory standards

Skills

Leadership
Strategic direction
Program management
Cross-functional collaboration
Risk management
Budgeting & forecasting
Vendor management

Education

Bachelor’s degree in science/health

Job description

Maze Therapeutics in South San Francisco seeks an Oversight Director, Clinical Operations to provide strategic and operational leadership across CKD and PKU programs from early development through pivotal studies. You will shape development strategy, oversee CRO/vendor relationships, and ensure high-quality trials on time and budget.

You will guide Study Leads and build a high-performing Clinical Operations team, driving risk management, resource planning, and regulatory readiness to support

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