Overview

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In this role, you drive end-to-end global 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
- Bachelor's degree
- At least 5 years of managing multinational clinical trials
- Sponsor-side experience
- Experience xqbhyrx leading general, 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

Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

📌 Single Sponsor Sr Clinical Project Manager (España)
🏢 Jobrapido
📍 España