Summary LOCATION: London, United Kingdom OR Dublin, Ireland 
 ROLE TYPE: Full Time, Permanent, Hybrid Working #LI-Hybrid 
 Step into a pivotal leadership role where your strategic vision and clinical expertise will shape the future of global drug development. 
 As Director of the Central Integrated Scientific Review Committee, you'll drive operational excellence across complex clinical programs, influence cross-functional teams, and foster a culture of empowerment and innovation. 
 Your work will directly contribute to accelerating access to life-changing treatments, improving patient outcomes worldwide, and setting new standards in clinical excellence. 
 
Key Responsibilities 
 Lead strategic and operational planning for assigned clinical programs from end to end 
 Oversee budget and resource allocation across global teams and clinical functions 
 Ensure quality and compliance across all clinical activities and program deliverables 
 Manage and develop high-performing teams in a matrixed, cross-functional environment 
 Drive process improvement initiatives and knowledge sharing across clinical operations 
 Collaborate with stakeholders to enhance operational and budget management capabilities 
 Represent the function in global initiatives, including SOP development and training 
 Ensure timely reporting of technical complaints and adverse events per regulatory standards 
Essential Requirements 
 Medical degree or advanced life sciences/healthcare qualification; PharmD or PhD strongly preferred 
 Demonstratable experience in a decision-making role within clinical research or drug development across Phases I-IV 
 Proven success in global clinical trial execution within a matrixed pharmaceutical environment 
 Strong leadership and people management capabilities across diverse, cross-functional teams 
 Excellent communication, negotiation, and conflict resolution skills 
 Demonstrated ability to influence without formal authority 
 Fluent in both written and spoken English 
 Deep understanding of regulatory standards and compliance in clinical operations 
 Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting, and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together? 
 Commitment to Diversity & Inclusion: 
 Novartis is committed to building an outstanding, inclusive work environment and diverse team's representative of the patients and communities we serve. 
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 Skills Desired Budget Management, Clinical Research, Clinical Trials, Coaching, Cross-Functional Teams, Lifesciences, People Management, Risk Management, Risk Monitoring               
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