Clinical Trial Manager, FSP Team — Drive Timely Data

ThermoFisher Scientific; Santiago; On-site; CLP 18,000,000 - 30,000,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Clinical Trial Manager for the FSP Team to drive pivotal study deliverables within contract terms. You will manage low to moderate complexity projects, ensuring data quality, regulatory compliance, and timely client updates.

The role requires collaboration across clinical operations, budgeting, and regulatory teams, with responsibilities that include development of monitoring tools and coordination of start-up activities.

Qualifications

• Bachelor's degree or equivalent and relevant formal academic/vocational qualification.
• 5+ years of experience in clinical trials or related field.

Responsibilities

• Oversee all clinical operational and quality aspects of allocated studies in compliance with ICH GCP.
• Develop and maintain clinical monitoring plans and trial master file documentation.
• Lead team meetings, track timelines, resources, and budgets to ensure on-time, within-scope delivery.
• Coordinate study start-up activities and regulatory submissions where applicable.
• Communicate with sites and internal stakeholders to resolve issues and ensure data quality.

Skills

Leadership

Project management

ICH/GCP knowledge

English proficiency

Budgeting

Regulatory knowledge

Communication

Education

Bachelor's degree in Life Sciences

Tools

MS Excel

MS Word

Outlook

Job description

Thermo Fisher Scientific is seeking a Clinical Trial Manager for the FSP Team to drive pivotal study deliverables within contract terms. You will manage low to moderate complexity projects, ensuring data quality, regulatory compliance, and timely client updates.

The role requires collaboration across clinical operations, budgeting, and regulatory teams, with responsibilities that include development of monitoring tools and coordination of start-up activities.