Local Study Operations Senior Manager

Career Category Clinical Development Job Description LOCAL STUDY OPERATIONS SENIOR MANAGER Responsibilities • Ensure the successful delivery of the study portfolio assigned to LSOMs. • Oversee LSOMs’ fulfillment of responsibilities throughout the assigned country portfolio, from feasibility through to study close-out. • Monitor portfolio progress, provide risk and quality oversight, and support issue escalation and resolution for LSOMs. • Manage LSOM and LSOM supplier performance to guarantee high-quality study execution, serving as the primary escalation point for local study challenges, driving solutions, and ensuring portfolio targets are met within the country. • Mentor, train, and support the professional development of LSOMs to prepare them for managing complex trials. • Build and maintain a high-performing team. • Facilitate close collaboration between the study strategy team and local study teams to effectively manage the assigned portfolio. • Promote cross-functional collaboration among country teams to ensure successful delivery of the country portfolio. • Support discussions regarding study placement decisions based on country capabilities and growth potential. • Proactively evaluate risks, quality trends, and resource requirements; implement mitigation strategies and drive continuous improvement in country operations. • Lead initiatives to enhance operational efficiency and encourage sharing of best practices. • Manage resource allocation and workload distribution across LSOMs, including both FSP and FTE personnel, to optimize trial execution and align with global priorities. • Ensure adherence to regulatory and quality standards where applicable. • Collaborate with and support the country head in engaging cross-functional stakeholders, aligning on trial deliverables, and managing escalations. Qualifications Minimum Requirements • Doctorate degree & 2 years of clinical execution experience OR • Master’s degree & 6 years of clinical execution experience OR • Bachelor’s degree & 8 years of clinical execution experience OR • Associate’s degree & 10 years of clinical execution experience OR • High school diploma / GED & 12 years of clinical execution experience • In addition to meeting at least one of the above requirements, you must have a minimum of 2 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources.

Your managerial experience may run concurrently with the required technical experience referenced above Preferred Requirements (based of GTM) • 7 years work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company • Experience managing multiple teams / direct reports across multiple clinical functions / trials • Experience at, or oversight of, clinical research suppliers (CRO’s, central labs, imaging suppliers, etc.) • Experience managing clinical operations across relevant geography / region, including strong understanding of local regulatory requirements around global clinical trials Competencies • Skilled in developing site-specific operational plans that enhance efficiency, compliance, and patient safety while implementing best practices and continuous improvement methodologies • Proficient in ensuring site preparedness and smooth execution across all study phases by supporting site initiation visits (SIVs), recruitment calls, and adherence to study timelines • Clear understanding of country level regulations and compliance for clinical trials, keeping up to date on clinical trial that may impacting managing ethics submissions, study start-up processes, and site inspection readiness at a country-level • Experience with developing and training teams related to clinical trial materials (e.g., CRAs, site staff, and cross-functional teams) to ensure alignment with study protocols, regulatory requirements, and best practices • Ability to identify operational risks based on protocol design and implement innovative mitigation strategies. Identify and manage study issues, communicating and/or escalating appropriately. • Demonstrates ability for end-to-end management of study deliverables, budgets, timelines, and performance metrics (KPIs) to optimize trial execution. • Experience with overseeing study budgets and financial operations, reviewing/approving site expenditures, and optimizing resource allocation to ensure cost efficiencies • Strong collaboration and communication skills to engage with cross-functional teams, senior management and external stakeholders, internally and externally • Able to identify and implement opportunities for continuous improvement into the team’s working practices • Navigates diverse regulatory, cultural, and operational environments.

Builds strong relationships across geographies and time zones. • Ability to manage, mentor, and develop professionals and support staff across functions, while fostering collaboration across internal and external teams for trial success .