Global Clinical Study Senior Manager

Scorpion Therapeutics; United States; On-site; USD 130,000 - 170,000; Full time

Job summary

Scorpion Therapeutics in the United States seeks a Lead Global Clinical Operations to drive end-to-end delivery of cancer-focused studies from start-up to close-out, overseeing planning, activation, enrollment, data management, and quality assurance.

You will coordinate cross-functional teams, liaise with external partners, ensure regulatory compliance, and develop SOPs. Travel may be required; strong leadership and communication skills are essential.

Qualifications

• Bachelor’s degree in scientific or healthcare field.
• 5+ years in clinical trial project management within biotech, pharma, or CRO sectors.
• Proven experience leading clinical functions in oncology or related therapeutic areas.
• Strong leadership, stakeholder management, and communication skills.

Responsibilities

• Oversee study planning, site activation, enrollment, data management, quality assurance, risk mitigation, and budget management.
• Coordinate cross-functional teams including medical, regulatory, biometrics, and supply.
• Serve as primary liaison to external partners and study teams.
• Ensure regulatory compliance and inspection readiness.
• Develop and optimize SOPs and work instructions.

Skills

Leadership

Stakeholder management

Communication

Cross-functional coordination

Regulatory awareness

Education

Bachelor’s degree in scientific/healthcare field

Tools

MS Office

Project planning tools

Job description

Role

Lead global clinical operations for one or more cancer-focused studies, ensuring end-to-end delivery from start-up to close-out.

Responsibilities

• oversee study planning, site activation, enrollment, data management, quality assurance, risk mitigation, and budget management
• coordinate cross-functional teams including medical, regulatory, biometrics, and supply
• serve as primary liaison to external partners and study teams
• ensure regulatory compliance and inspection readiness
• develop and optimize SOPs and work instructions.

Requirements

• Bachelor's in a scientific or healthcare discipline
• 5+ years in clinical trial project management within biotech, pharma, or CRO sectors
• proven experience leading clinical functions in oncology or related therapeutic areas
• strong leadership, stakeholder management, and communication skills.

Preferred

• higher degree
• experience with international oncology trials, GxP standards, and clinical systems (MS Office, project planning tools).

High-value biopharma specifics

oncology focus, global scope, cross-regional study management, study start-up and enrollment expertise, regulatory compliance, and vendor oversight.

Collaboration/reporting

interacts with BU Clinical Operations Lead, Biotech Unit Leadership, and cross-functional teams.

Work setup

• travel may be required
• location modality not specified.