Associate Director / Director Global Clinical Process Management Lead

BeOne Medicines Ltd.; United States; On-site; USD 140,000 - 185,000; Full time

Job summary

Scorpion Therapeutics seeks a Global Clinical Process Management Lead within GCO to standardize and optimize global clinical processes, ensuring adherence to GCP and regulatory standards. The role emphasizes cross-functional collaboration, SOP governance, and continuous improvement in a matrix, primarily remote setting.

The position requires extensive experience in clinical operations, with a strong focus on process design, governance, and stakeholder coordination to drive harmonization across

Qualifications

• Bachelor's degree in science or healthcare preferred.
• Minimum 8 years in pharmaceutical/biotech sector.
• Extensive knowledge of clinical operations, GCP, and regulation.

Responsibilities

• Oversee process management activities in global clinical operations.
• Serve as primary contact for GCO processes including SOPs and Work Instructions.
• Contribute to content development and lead process initiatives.
• Support innovative process improvements aligned with regulatory standards (ICH-GCP).

Skills

Project management

Stakeholder collaboration

Process design

Regulatory compliance

Communication

Organizational skills

Problem-solving

Education

Bachelor's degree (science/healthcare preferred)

Job description

Role

Global Clinical Process Management Lead within GCO, responsible for leading and supporting clinical process standardization, compliance, and continuous improvement in global clinical operations.

Responsibilities

oversee process management activities, serve as the primary contact for GCO processes including SOPs and Work Instructions, contribute to content development, lead process initiatives, and support innovative process improvements aligned with regulatory standards (ICH-GCP).

Qualifications

Bachelor's degree (science/healthcare preferred), minimum 8 years in pharmaceutical/biotech sector, extensive knowledge of clinical operations, GCP, and regulation application.

Skills

strong project management, stakeholder collaboration, process design, and regulatory compliance experience, with excellent communication, organizational, and problem-solving capabilities.

Preferred

master’s or postgraduate qualification.

High-Value

experience in clinical trial process design and harmonization, global matrix environment, regulatory compliance, and process improvement.

Work setup

primarily remote with matrix supervisory responsibilities.