Director, Process Optimization Lead

General Description:Responsible for the business operations of the Program and Study Management (P&SM) function, driving operational excellence, innovation, and continuous process improvement from strategic planning through implementation. This could include managing initiatives, organizing meetings, overseeing budgets, optimizing processes, managing resources, setting and tracking goals, and performing other assigned duties.Actively participates in shaping the P&SM strategy while leading and engaging in functional management activities. Utilizes strategic thinking across various roles within the global P&SM team and at the Global Clinical Operations (GCO) level to significantly influence long-term strategic direction.Identifies process optimization opportunities to enhance team working efficiency and improve the quality of business delivery. Collaborates with the P&SM team, other GCO functional teams, and cross-functional teams on process optimization and strategy alignment at both regional and global levels, ensuring that operational processes effectively meet business needs.Inspires and leads initiatives to enhance the necessary technical skills and competencies within the Global Clinical Study Management team, facilitating more efficient clinical study execution while ensuring patient safety, compliance, and data integrity through optimized operational processes.Provides expert knowledge regarding the execution of clinical studies and demonstrates a thorough understanding of ICH/GCP guidelines and other relevant regulatory requirements.Establishes and enhances BeOne's reputation, capability, and capacity for successfully delivering clinical studies.Essential Functions of the Job:Functional Support and Operational ExcellenceIdentify key areas for improvement in operational practices, conduct root cause analyses, and develop improvement plans in collaboration with P&SM team, GCO sub-functions, and cross-functional teams independently.Lead initiative management and process optimization activities to drive operational excellence within the P&SM function by fostering innovation and promoting continuous process improvement.Contribute to shaping the overall P&SM strategy and support functional management activities while applying strategic thinking across various roles in the global P&SM team to influence long-term strategy and organizational decision-making processes.Strategic Leadership and Cross-Functional InfluenceWork with the Optimization Head of P&SM to define and implement strategies and key priorities in collaboration with GCPL and gCSM groups, supporting global study teams in executing clinical studies.Collaborate with P&SM groups, GCO sub-teams, and other cross-functional teams on process optimization initiatives, development of implementation plans, and tracking results.Ensure alignment with BeOne's broader strategic goals and business needs.Shaping Relationships and Thought LeadershipChampion and promote a global mindset to enhance collaboration and consistency across BeOne.Present and articulate information in a composed and confident manner.Provide strategic recommendations and innovative ideas to generate greater value for BeOne overall.Proactively escalate issues to the BeOne Senior Management team with a solutions-oriented approach.Contribute to the development of training plans and programs aimed at enhancing clinical project management skills, fostering a culture of continuous learning.Supervisory Responsibilities:NAComputer Skills:Proficiency in MS Office Suite, including Excel, PowerPoint, and Project ect.Other Qualifications:Bachelor or higher degrees (life science preferred, including medicine, nursing, biology, and laboratory technology)Fluent in written and verbal English10 years or above in clinical or drug development in the biotech/pharmaceutical/CRO industry or the relevant clinical research fieldMinimum of 8 years of project management and/or clinical monitoring/ or start-up experienceTravel:Travel as required per business needsEducation Required :BS or higher degrees. 10 years or above in clinical or drug development in the biotech/pharmaceutical/CRO industry or the relevant clinical research field. Minimum of 8 years of project management and/or clinical monitoring/ or start-up experience*exceptions might be made for candidates with relevant clinical operations experienceAll qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.