FSP Sr CM Analyst II

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.
Apply today to help us deliver tomorrow’s breakthroughs.

Skills
Data Analysis, Regulatory Compliance