Senior Clinical Trial Manager

🔥 1 hour ago

🇪🇸 Spain – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

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AbbVie

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2013

🏥 Healthcare

💼 Consulting

🏭 Manufacturing

Healthcare • Consulting • Manufacturing

AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.

📋 Description

• Plan, execute, and manage one or more Phase 0–4 global clinical trials • Provide study-level oversight and leadership from trial inception through closure • Support cross-functional team leadership, stakeholder engagement, strategy development, meeting facilitation, and documentation • Manage external vendors, including RFPs, vendor selection, scopes of work, deliverables, and risk management • Lead global recruitment strategies, feasibility activities, subject recruitment, retention, and mitigation planning • Lead cross-functional, vendor, and investigator meetings and provide regular study-status updates • Ensure inspection readiness and participate in related activities • Identify, mitigate, escalate, and manage study risks • Co-develop and manage protocols, regulatory submissions, informed consent, study plans, budgets, agreements, clinical study reports, training materials, newsletters, and presentations • Manage CTMS and eTMF to support compliance, inspection readiness, trend analysis, and timelines • Support EDC, IRT, and ePRO design reviews, user acceptance testing, associated plans, risk indicators, access support, query resolution, and system oversight • Manage investigational product and study supplies • Provide stakeholder training • Support global submission strategies • Support process improvement initiatives and serve as a subject matter expert or mentor

🎯 Requirements

• Bachelor’s Degree or OUS equivalent required • At least 4 years of progressive pharma-related or clinical research-related experience • Competence in standard quality procedures, including SOP, ICH/GCP, and Global Regulations • Experience with EDC, IRT, CTMS, and eTMF systems • Strong analytical and critical thinking skills • Excellent organizational and time management skills • Strong attention to detail • Exceptional interpersonal and communication skills in a global setting • Proficient in business/technical English, oral and written • Proactive, collaborative mindset • Ability to work independently in a fast-paced global team environment

🏖️ Benefits

• Remote work arrangement • Equal opportunity employment • Integrity-driven workplace • Innovation-focused workplace • Community service commitment

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