Global Clinical Delivery Lead & Stakeholder Strategist

Kaufmann; Pudahuel; On-site; CLP 117,763,000 - 147,203,000; Full time

Job summary

Kaufmann is seeking a Clinical Lead to oversee delivery of global clinical studies, ensuring milestones, budgets, and quality standards are met. The role collaborates with cross-functional teams and external partners to deliver trials efficiently from initiation to closeout.

The position requires leading clinical teams, managing recruitment, and applying regulatory knowledge to ensure compliant trial conduct across regions, including site visits and bid preparations.

Qualifications

• Bachelor's Degree in health care or life science.
• 5 years clinical research/monitoring experience or equivalent.
• Knowledge of GCP/ICH guidelines and regulatory requirements.
• Understanding of project finances and budgeting.
• Strong written and verbal communication in English.

Responsibilities

• Ensure clinical delivery in compliance with regulatory requirements (GCP/ICH) and SOPs.
• Meet recruitment targets and implement recruitment strategies.
• Develop and manage risk mitigation plans for clinical projects.
• Ensure clinical quality and measurement of compliance across projects.
• Manage project finances, including Estimate at Completion (EAC).
• Identify clinical stakeholder landscape and manage internal/external communications.
• Lead clinical teams and provide guidance and trainings at project level.
• Mentor peers and contribute to clinical delivery strategy.
• Support bid defenses and participate in proposal development.
• Attend site visits as applicable to project delivery.

Skills

Clinical research

Project management

Regulatory knowledge

English communication

Leadership

Microsoft Office

Education

Bachelor's degree in health care or life sciences

Tools

Microsoft Word

Excel

PowerPoint

Job description

Kaufmann is seeking a Clinical Lead to oversee delivery of global clinical studies, ensuring milestones, budgets, and quality standards are met. The role collaborates with cross-functional teams and external partners to deliver trials efficiently from initiation to closeout.

The position requires leading clinical teams, managing recruitment, and applying regulatory knowledge to ensure compliant trial conduct across regions, including site visits and bid preparations.