Global Clinical Operations Lead: Trials & Site Strategy

SanegeneBio Inc.; China (TX); Hybrid; USD 120,000 - 190,000; Full time

Job summary

SanegeneBio is seeking an experienced Clinical Operations professional to support global trials across the U.S. and China.

The role drives study delivery through cross-functional coordination, vendor management, and operational oversight from start-up to close-out, ensuring high-quality, timely, and compliant execution. You will lead trial operations in China and overseas, contribute to development plans and protocols, manage sites and vendors, draft essential documents, and monitor budgets and

Qualifications

• Background in biochemistry, medicine, or related life science disciplines.
• More than 6 years of clinical trial operations and project management experience.
• Strong professional writing skills, including regulatory documentation.
• Proficient in English communication, reading, and writing.

Responsibilities

• Manage clinical trial projects in China and overseas, including monitoring study progress, quality, and budget execution.
• Participate in the development of overall clinical development plans and clinical trial protocols.
• Lead the selection and evaluation of clinical trial sites, CROs, SMOs, and other service providers.
• Draft, review, and finalize key clinical trial documents, including study protocols, source documents, CRFs, and trial manuals.
• Develop project management plans in accordance with study protocols, including team allocation and budget planning.
• Establish and maintain effective collaboration with investigators, clinical sites, CROs, SMOs, and other vendors.
• Communicate with cross-functional stakeholders and provide regular updates on study progress.

Skills

Regulatory writing

Clinical trial operations

Project management

Cross-functional coordination

English proficiency

Job description

SanegeneBio is seeking an experienced Clinical Operations professional to support global trials across the U.S. and China.

The role drives study delivery through cross-functional coordination, vendor management, and operational oversight from start-up to close-out, ensuring high-quality, timely, and compliant execution. You will lead trial operations in China and overseas, contribute to development plans and protocols, manage sites and vendors, draft essential documents, and monitor budgets and