MadridFull TimeOperations
Remotely
clinical trialssite monitoringmicrosoft excelmicrosoft wordmicrosoft powerpointramptmfdata cleaning
Job Description
📋 Description
- Lead CSM strategy across studies; ensure integrity, quality and timely deliverables.
- Drive site selection, activation, engagement, protocol adherence and close-out at study/area level.
- Oversee monitoring activities; ensure quality deliverables and milestone adherence.
- Provide study information to country teams to enable milestones; manage data snapshots and DB locks.
- Identify and mitigate risks; contribute to Risk Assessment and Mitigation Plan (RAMP).
🎯 Requirements
- Bachelor’s Degree or equivalent in a medical/scientific field; 5+ years clinical research; global
- Experience in study initiation through completion; ability to influence in matrix environments.
- Proficient in SOPs, ICH, global regulations; fluent English; strong presentation and organizational
- Strong communication, leadership, and ability to work autonomously in fast-paced settings.
- Advanced skills in Word, PowerPoint, Excel, OneNote.
🎁 Benefits
- Health care coverage and related AbbVie benefits.
- Equal opportunity employer; commitment to integrity and innovation.
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