Overview
In this role, you drive end-to-end integral clinical trial management on sponsor-supported programs, ensuring timely delivery and regulatory readiness. You will collaborate with cross-functional teams to oversee trial timelines, budgets, site feasibility, vendor management, and supply planning. You'll apply your therapeutic-area expertise in Oncology, Hematology, or Immunology to lead pivotal studies across regions. This is a globally focused, impactful role within a mission-driven, performance-driven organization.
Compensaciones / Beneficios career development and progression
supportive line management
technical and therapeutic area training
peer recognition
total rewards program
inclusive culture
Responsabilidades Assess and develop clinical trial documents and regulatory paperwork (protocols, CRFs, informed consent forms, CSR)
Oversee site feasibility, investigator selection, and vendor activities
Manage trial timelines, budgets, data review,



and discrepancy resolution
Coordinate clinical trial supply plans and recruitment/risk mitigation strategies
Monitor and adjust contingency plans across global, multi-regional studies
Ensure compliance with regulatory requirements and sponsor expectations
Requisitos principales Bachelors degree
At least 5 years of managing multinational clinical trials
Sponsor-side experience
Experience leading global, multi-regional studies
Therapeutic-area expertise in Oncology, Hematology, or Immunology
Experience with complex or pivotal studies
collaboration with diverse teams
problem solving and adaptability
strong communication and stakeholder management
clinical trial document development and writing
feasibility assessment
vendor management

📌 Single Sponsor Sr Clinical Project Manager (Valencia)
🏢 Syneos Health
📍 Valencia