19 sep
|
Syneos Health
|
Valencia
19 sep
Syneos Health
Valencia
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.
supportive line management
technical and therapeutic area training
Responsabilidades Assess and develop clinical trial documents and regulatory paperwork (protocols, CRFs, informed consent forms, CSR)
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
Requisitos principales Bachelors degree
At least 5 years of managing multinational clinical trials
Experience leading global, multi-regional studies
Therapeutic-area expertise in Oncology, Hematology, or Immunology
strong communication and stakeholder management
clinical trial document development and writing
vendor management
📌 Single Sponsor Sr Clinical Project Manager (Valencia)
🏢 Syneos Health
📍 Valencia