Overview In this role, you drive end-to-end general 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 (Global exp) Fully home based in Bulgaria, Spain, UK or P (León)
🏢 Syneos Health
📍 León