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 (Castilla-La Mancha)
🏢 Syneos Health
📍 Castilla-La Mancha