Clinical Trial Manager: Lead Global Trials & Data

ThermoFisher Scientific; United States; Remote; USD 110,000 - 150,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Clinical Trial Manager to lead the operational and quality aspects of studies, ensuring timely, within-scope deliverables and profitability. You will collaborate with cross-functional teams, prepare site communications, and oversee monitoring processes to meet client expectations.

Ideal candidates bring strong leadership, budgeting, and regulatory knowledge, with experience in ICH/GCP and FDA guidelines, and willingness to travel domestically and

Qualifications

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification.
• 5+ years of relevant clinical trial experience.
• Equivalency may be considered to meet role requirements.

Responsibilities

• Manage clinical operational and quality aspects of allocated studies (low to moderate complexity) following ICH GCP.
• Develop monitoring plans and templates in conjunction with the Data Quality Plan and MAP.
• Coordinate with project team to prepare, organize and present at client meetings.
• Lead team meetings to ensure timelines, resources and quality; implement standardized monitoring processes.
• Monitor or co-monitor trials, manage CRF collection and query resolution, and track progress.
• Support start-up activities and ensure regulatory submissions where appropriate.

Skills

Leadership

Planning

Interpersonal Skills

Problem Solving

Multicultural Collaboration

Monitoring Knowledge

Decision Making

Communication

Budgeting

Attention to Detail

Regulatory Knowledge

Computer Skills

Education

Bachelor's degree or equivalent

5+ years of clinical trial experience

Job description

Thermo Fisher Scientific is seeking a Clinical Trial Manager to lead the operational and quality aspects of studies, ensuring timely, within-scope deliverables and profitability. You will collaborate with cross-functional teams, prepare site communications, and oversee monitoring processes to meet client expectations.

Ideal candidates bring strong leadership, budgeting, and regulatory knowledge, with experience in ICH/GCP and FDA guidelines, and willingness to travel domestically and