FSP Sr CM Analyst II

ThermoFisher Scientific; Chile; Remote; CLP 8,000,000 - 12,000,000; Full time

Job summary

Thermo Fisher Scientific in Chile is seeking a Sr CM Analyst II Trial Data Analytics Specialist to drive operational excellence in clinical trials. You will identify issues and trends in patient data, perform risk assessments, and collaborate with cross-functional teams to develop findings and action plans.

The role demands strong communication, leadership, and knowledge of site monitoring and regulatory compliance.

Qualifications

• Degree in Life Sciences or related field or equivalent experience.
• Strong knowledge of Site Monitoring and Site Management.
• Experience working with cross-functional teams and leadership capabilities.

Responsibilities

• Risk assessments.
• Monitoring plans.
• Sponsor oversight.
• Trend analysis.
• Signal detection.
• Site monitoring strategy.
• Regulatory compliance.
• Inspection readiness.

Skills

Site Monitoring

Site Management

Cross-functional teams

Leadership

Communication skills

Education

Degree in Life Sciences or related field

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Sr CM Analyst II– Make an Impact at the Forefront of Innovation

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Trial Data Analytics Specialist II, you will identify and characterize issues and trends in operational and patient clinical trial data using analytical or statistical tools. You will leverage your operational experience and knowledge to evaluate issues and develop findings based on the data analyzed, communicating issues and potential risks to project team members for follow-up action.

• Model: Functional Service Partnership (FSP), dedicated to a specific pharmaceutical client.
• Key Responsibilities: Risk assessments, monitoring plans, sponsor oversight, trend analysis, signal detection, site monitoring strategy, regulatory compliance, and inspection readiness.
• Qualifications: Degree in Life Sciences or a related field, or equivalent professional experience as permitted by the approved job description. Strong knowledge of Site Monitoring and Site Management, communication skills, leadership capabilities, and experience working with cross-functional teams.
• Experience: 3 years, as indicated in the client's job description, subject to confirmation against the requirements for the Sr CM Analyst II level.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.