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 general 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