Experteer Overview In this role you will lead clinical programs by linking science with operations to execute studies at high quality and with efficiency. You will act as a strategic advocate for pipeline assets and shape operational plans that connect science, business, patients, and customers. You’ll mentor a development-oriented team and drive risk management, budgets, and regulatory compliance across integral studies. The position sits at the intersection of clinical development and operations, offering the opportunity to influence multi-phase programs and enable therapeutic breakthroughs. This is a chance to help AbbVie deliver medicines that improve patients’ lives at scale while fostering an inclusive, inCompensaciones / Beneficios
- Develop clinical operational strategy and ensure programs are executed on-time, within budget, and to company objectives
- Translate asset strategy into operational execution by developing the clinical operations plan and connecting science with business, operations, patients and customers
- Identify and evaluate program-level risks and mitigations
- Interact with and influence senior management and cross-functional teams to meet program objectives
- Review and provide clinical operations content to clinical and regulatory documents
- Manage external budgets across portfolios (up to multi-million dollars)
- Mentor and develop study managers; lead talent developmentin Development Operations
- Create an inclusive, innovative learning environment for staff and programs
- Ensure program execution in compliance with ICH/GCP, global regulations, and AbbVie policies
- Communicate effectively with stakeholders and drive activities even with incomplete informationResponsabilidades
- 12+ years of Pharma-related/clinical research experience
- 8+ years in clinical research demonstrating leadership and strategic impact
- Proven ability to lead a global team on multiple complex studies
- COaching/mentoring and people management experience (remote management preferred)
- Expertise in SOPs, ICH, global regulations, ethics and compliance
- Experience in study initiation through completion across phases (Phase 1-3, 4)
- Strong communication and stakeholder management skillsRequisitos principales
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📌 Program Lead Ii, Clinical Program Development (Madrid)
🏢 Abbvie
📍 Madrid