Senior Clinical Trial Leader — Drive Global Impact

ThermoFisher Scientific; United States; Remote; BRL 300,000 - 540,000; Full time

Job summary

Thermo Fisher Scientific in Brazil is seeking a Senior Clinical Trial Manager to lead clinical operations and ensure timely, high-quality data delivery within contract scopes. The role requires independent management of moderate to high complexity trials and regional leadership duties where applicable.

You will drive monitoring plans, oversee TMF integrity, and coordinate cross-functional teams to meet timelines and budgets while maintaining compliance with ICH GCP and FDA guidelines.

Qualifications

• Bachelor's degree or equivalent and relevant formal academic/vocational qualification.
• 8+ years of relevant experience in clinical trials.
• Equivalency may be considered with appropriate education or directly related experience.

Responsibilities

• Manage all clinical operational and quality aspects of allocated studies in compliance with ICH GCP.
• May assume Lead CTM or Clinical Study Manager responsibilities on regional level.
• Collaborate with the project team to prepare, organize, and present at client meetings.
• Ensure timely archiving of documents and study materials.
• Provide input into forecast estimates for clinical activities.
• Oversee resource management and budgeting for clinical projects.

Skills

Leadership

Planning

Communication

Regulatory knowledge

Budgeting

Change management

Clinical monitoring

Mentoring

Education

Bachelor's degree or equivalent

8+ years in clinical trials

Tools

Microsoft Outlook

Excel

Word

Job description

Thermo Fisher Scientific in Brazil is seeking a Senior Clinical Trial Manager to lead clinical operations and ensure timely, high-quality data delivery within contract scopes. The role requires independent management of moderate to high complexity trials and regional leadership duties where applicable.

You will drive monitoring plans, oversee TMF integrity, and coordinate cross-functional teams to meet timelines and budgets while maintaining compliance with ICH GCP and FDA guidelines.