Clinical Trial Manager - Adult Psychiatry

Centro De Salud Mental Raíces; Santiago; On-site; CLP 89,463,000 - 129,225,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Sr CTM to lead clinical trial management activities, ensuring timely, quality, and cost-effective delivery of clinical data. You will oversee teams, develop essential monitoring tools, and coordinate with sites and stakeholders to meet contractual obligations.

The role requires strong leadership, planning, and regulatory knowledge, with experience in ICH/GCP guidelines and an ability to work in a global, matrixed environment.

Qualifications

• Bachelor's degree or equivalent and relevant formal academic/vocational qualification.
• 5+ years of experience in clinical trial management or related field.
• Equivalency of education, training, and experience may be considered.

Responsibilities

• Manage all clinical operational and quality aspects of allocated studies in compliance with ICH GCP.
• Develop monitoring plans and contribute to the Master Action Plan for clinical documentation.
• Coordinate start-up activities and ensure timely ethical and regulatory submissions where applicable.
• Monitor timelines, track metrics, and manage resource allocation to meet contractual obligations.
• Communicate with study sites regarding protocol, patient participation, and data quality.

Skills

Leadership

Planning & Organizing

Interpersonal Skills

Problem Solving

English Proficiency

Budgeting & Forecasting

Attention to Detail

Regulatory Knowledge

Computer Skills

Education

Bachelor's degree or equivalent

Tools

MS Office

Outlook

Excel

Word

Job description

Thermo Fisher Scientific is seeking a Sr CTM to lead clinical trial management activities, ensuring timely, quality, and cost-effective delivery of clinical data. You will oversee teams, develop essential monitoring tools, and coordinate with sites and stakeholders to meet contractual obligations.

The role requires strong leadership, planning, and regulatory knowledge, with experience in ICH/GCP guidelines and an ability to work in a global, matrixed environment.