Site Management Lead - (Clinical Research) (Madrid)

Site Management Lead - (Clinical Research) (Madrid)

02 sep
|
Abbvie
|
Madrid

02 sep

Abbvie

Madrid

Experteer Overview
In this role you will steer Clinical Site Management (CSM) for global studies, ensuring timely, compliant site activities and study deliverables. You will lead or co-lead CSM strategy, collaborate with cross-functional teams, and manage risks and TMF readiness. You’ll drive site selection, activation, engagement, and close-out, shaping how trials run across regions. This is a high-impact position that supports AbbVie’s mission to deliver innovative medicines by optimizing study execution at scale.

Compensaciones / Beneficios
• Analyze study timelines and feasibility for CSM deliverables
• Communicate and align CSM resource needs with country leaders
• Own study-level site monitoring strategy and Site Monitoring Plan
• Lead Site Engagement Strategy and maintain study-level timelines
• Drive site-level activities (selection, activation, engagement, protocol adherence, close-out)
• Oversee monitoring activities across study/area levels with quality and milestone tracking
• Support data snapshots and database locks per the Data Cleaning Plan
• Ensure site closures per Site Closure Plan
• Identify, evaluate, and mitigate risks; contribute to RAMP




• Collaborate with SMLs and stakeholders to address risks and ensure execution
• Ensure CSM artifacts TMF completeness and inspection readiness across the study
• Maintain ongoing CSM compliance and issue escalation in a matrix environment
• Prepare and deliver CSM inputs for study-level documentation

Responsabilidades
• Bachelor's degree or equivalent in a (para)medical or scientific field
• minimum 5 years of industry clinical research experience
• preferably 2 years in monitoring or project management on a global study
• experience across Phase II/III (and Phase I in patients) and multiple therapeutic areas
• strong communication and leadership abilities; ability to influence without authority
• familiarity with SOPs, ICH, General Regulations, Ethics and Compliance
• excellent written and verbal English; strong planning and organizational skills
• ability to create and deliver presentations; works well in matrix teams and autonomously
• proficient in Microsoft Word, PowerPoint, Excel, OneNote

Requisitos principales


📌 Site Management Lead - (Clinical Research) (Madrid)
🏢 Abbvie
📍 Madrid

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