Site Management Lead - (Clinical Research) (Madrid)

Site Management Lead - (Clinical Research) (Madrid)

31 ago
|
Abbvie
|
Madrid

31 ago

Abbvie

Madrid

Experteer Overview

Asegúrese de enviar su solicitud rápidamente para maximizar sus posibilidades de ser considerado para una entrevista. Lea la descripción completa del puesto a continuación.

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 xugodme or project management on a general 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, Global 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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