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Job Description
📋 Description Advance AbbVie’s pipeline in clinical research and drive industry-leading performance. Partner with investigators and site staff for effective engagements and data integrity. Focus on site conduct, trial safety, and patient experience across regulatory requirements. Serve as primary site contact, align sites with trial goals and patient treatment principles. Monitor site evaluation/training, ensure protocol compliance and GCP adherence. Develop site engagement strategy and report progress using CRM tools. 🎯 Requirements Healthcare/clinical-related qualification (medical, scientific, nursing) or equivalent experience. Experience in clinical research coordination or data management preferred. Knowledge of regulatory/ICH/GCP guidelines and site-based processes. Strong planning, organizational, and cross-functional collaboration skills. Ability to apply critical thinking to address site issues and drive protocol compliance. Excellent communication, relationship-building, and stakeholder management skills. 🎁 Benefits AbbVie benefits package including PTO and health coverage. Eligibility for short-term incentive programs. Equal opportunity employer with comprehensive rewards and recognition.
