Head- Contract Management

In this vital and influential role, the Global Head of Site Contracting has overall accountability for the site contracting process at Novartis, with a focus on optimizing cycle time and efficiency and thinking strategically about Novartis’ approach to contract execution in support of industry leading study start-up timelines. Working across the matrix of stakeholders that impact contract execution, they will design, implement, manage and monitor contracts and grants workflow procedures and tools and ensure appropriate data and metrics are in place for both operational study level delivery and process control. They will not have day to day oversight of operational contract execution at a study or portfolio level. In addition, this leadership role has direct line management responsibility for the Study Grants team and is accountable for providing Grant Plans and Fair Market Value assessments for all Globally, Locally and Regionally Supported Clinical Trials and Investigator Initiated Trials. Lead the design, implementation and ongoing management of contracts and grants workflow, process, tools and technology Ongoing proactive assessment of Novartis process, tools and technology as it pertains to contract execution, with a focus on cycle time optimisation and efficiency Ensure contracting process is compliant with appropriate quality standards and regulations and leads any associated actions required Establish strong working relationships across the matrix of stakeholders that impact contract execution to harness their expertise in line with goals Ensure appropriate data and metrics are in place to provide timely insights for both operational study level delivery and process control. Maintain a strong understanding of external best practice and clinical trial landscape factors that could impact contract execution Lead the design and implementation of Novartis’ Grant Plan strategy and Fair Market Value (FMV) assessments in support of clinical trials. Oversee quality and timely translation of clinical protocol visit assessment schedule into intelligent Grant Plan and FMV cost estimations, ensuring clinical operational and scientific requirements are reflected accurately. Bachelor’s degree in life science, business or operations ~10+ years of pharmaceutical industry experience, with previous significant experience in site contracts ~ Strong leadership and people management skills in a global setting with proven ability to develop high-performing teams and diverse profiles. ~ Proven expert level knowledge of and experience with operational management, and exceptional technical, analytical and quantitative problem-solving skills. ~ Credible and confident at building relationships at the leadership level while demonstrating organizational agility. ~ Experience working with electronic databases, clinical and/or project management planning and reporting and analytics systems. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. #