CRA I/ II- FSP - Spain

Thermo Fisher Scientific seeks a Clinical Research Associate to monitor investigational sites for a dedicated pharmaceutical client partnership in Madrid. The role involves conducting remote and on-site visits to ensure protocol compliance, manage documentation, and support clinical trial operations while working within a global organization committed to career development.

Responsibilities

• Conduct remote and on-site site monitoring visits using risk-based approaches and root cause analysis
• Review source documents, case report forms, and investigational product records for accuracy and compliance
• Initiate clinical trial sites and perform trial closeout activities according to protocol and regulatory requirements
• Ensure essential regulatory documents are complete and prepare trial status reports for clinical management
• Facilitate communication between investigative sites, sponsor, and project team; respond to audits and inspections

Requirements

• Bachelor's degree in life sciences or registered nursing certification with equivalent qualification
• 1–3 years of clinical research monitoring experience
• Oncology studies experience required
• Proven clinical monitoring skills and risk-based assessment capabilities
• Valid driver's license where applicable
• Strong written and oral communication abilities