Global Oncology Clinical Operations Lead, Phase 2/3

Scorpion Therapeutics

Miami (FL)

On-site

USD 170,000 - 210,000

Full time

11 days ago
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Job summary

Scorpion Therapeutics seeks an Associate Director of Clinical Operations to lead global oncology Phase 2/3 trials, including NSCLC and CRC, with a strong focus on execution and vendor management.

You will oversee trial planning, ensure GCP/ICH compliance, manage CROs, control budgets, and maintain inspection readiness while driving cross-functional collaboration with Regulatory, Clinical Science, Data Management, and Quality teams. Travel up to 20% is expected.

Qualifications

  • 10+ years of experience managing international oncology clinical trials.
  • Strong leadership, regulatory and operational expertise.
  • Experience overseeing CROs and external vendors.

Responsibilities

  • Oversee clinical trial planning and execution for global oncology trials.
  • Ensure compliance with GCP/ICH guidelines and regulatory requirements.
  • Manage CROs and external vendors, including vendor selection and performance monitoring.
  • Mitigate operational risks and control trial budgets.
  • Maintain inspection readiness and TMF quality across studies.
  • Foster cross-functional collaboration with Regulatory, Clinical Science, Data Management, and Quality teams.
  • Lead development and approval of study plans and TMF artifacts.
  • Drive process improvements in Clinical Operations.

Skills

Leadership
Regulatory expertise
Operational management
Budget management
Vendor management
GCP/ICH compliance
Cross-functional collaboration

Education

Bachelor's degree in life sciences or related field

Job description

Scorpion Therapeutics seeks an Associate Director of Clinical Operations to lead global oncology Phase 2/3 trials, including NSCLC and CRC, with a strong focus on execution and vendor management.

You will oversee trial planning, ensure GCP/ICH compliance, manage CROs, control budgets, and maintain inspection readiness while driving cross-functional collaboration with Regulatory, Clinical Science, Data Management, and Quality teams. Travel up to 20% is expected.

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