Gestor de Ensayos Clínicos FSP - Lidera Proyectos

Nurse Service; Santiago; On-site; CLP 9,000,000 - 15,000,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Sr CTM to oversee clinical operations for low to moderate complexity studies in Santiago. The role drives data quality, adherence to contract scope, and team leadership to deliver on patient data and milestones.

You will collaborate with cross-functional teams, coordinate start-up activities, monitor timelines, and ensure compliance with ICH/GCP and FDA guidelines while managing resources and sponsor expectations.

Qualifications

• Bachelor's degree or equivalent and relevant formal academic qualification.
• 5+ years of experience in Clinical Trial Management or equivalent.
• Experience with regulatory guidelines (ICH/GCP, FDA) preferred.

Responsibilities

• Manage all clinical operations and quality aspects of allocated studies in compliance with ICH GCP.
• Develop clinical tools (e.g., Monitoring Plan) and support Master Action Plan development.
• Coordinate start-up activities and regulatory submissions as appropriate.
• Ensure timely clinical activity timelines, budgets, and resource management.
• Maintain documentation quality and conduct regular status reviews with project manager.

Skills

Leadership

Planning

Interpersonal

English proficiency

Budgeting

Problem solving

Education

Bachelor's degree

Tools

Outlook

Excel

Word

Job description

Thermo Fisher Scientific is seeking a Sr CTM to oversee clinical operations for low to moderate complexity studies in Santiago. The role drives data quality, adherence to contract scope, and team leadership to deliver on patient data and milestones.

You will collaborate with cross-functional teams, coordinate start-up activities, monitor timelines, and ensure compliance with ICH/GCP and FDA guidelines while managing resources and sponsor expectations.