Senior Clinical Operations Lead - Trials & Strategy

Remote DXB; United States; Remote; USD 180,000 - 240,000; Full time

Job summary

Generate:Biomedicines is seeking a senior Clinical Operations leader to shape and oversee the strategy for programs in development. You will partner with cross-functional teams to drive protocols, safety reports, investigator brochures, and regulatory submissions.

The role includes evaluating CROs and sites, negotiating scopes of work and budgets, and ensuring GCP-compliant SOPs while coordinating study timelines with clinical development, pharmacology, data management, and regulatory affairs.

Qualifications

• Minimum 8 years of experience in clinical operations across at least two therapeutic areas, including oncology.
• Experience managing CROs and vendors for US and international trials.
• Strong ability to communicate in a fast-paced, collaborative environment.

Responsibilities

• Develop clinical operations strategy for programs in development
• Collaborate cross-functionally to develop protocols, safety reports, investigator brochures, and regulatory submissions
• Evaluate and select CROs and sites, developing scopes of work, contracts, and budgets
• Develop and manage SOPs and ensure GCP compliance
• Manage study timelines in coordination with clinical development, pharmacology, data management, and regulatory affairs
• Lead patient recruitment planning and forecasting
• Manage and mentor Clinical Operations team members

Skills

Clinical operations

CRO/vendor management

Regulatory submissions

Protocol development

Study management

Team leadership

Communication

Job description

Generate:Biomedicines is seeking a senior Clinical Operations leader to shape and oversee the strategy for programs in development. You will partner with cross-functional teams to drive protocols, safety reports, investigator brochures, and regulatory submissions.

The role includes evaluating CROs and sites, negotiating scopes of work and budgets, and ensuring GCP-compliant SOPs while coordinating study timelines with clinical development, pharmacology, data management, and regulatory affairs.