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The Director / Senior Director, Project Management :
Provides direct support for global R&D and non-R&D activities
Partners with VP of Pipeline Value Up to provide financial oversight of R&D budgets
Assists VP of Pipeline Value Up on ad-hoc requests received from the CEO and Senior Leadership as needed to support company initiatives
Responsibilities :
Driving alignment, collaboration, accountability and milestone achievement within project team(s)
Fostering strong relationships and supporting effective and impactful communications with management, team members and functional line managers in order to ensure active management of issues / risks / decisions / opportunities
Assisting VP of Pipeline Value Up with fiscal responsibilities to support management of financial aspects of programs including tracking to budget and ensuring effective use of resources throughout the year
Communicating to and interacting with SKBP / SKLSI Management to ensure appropriate flow of project information to decision makers in Korea
Ensuring that team discussions drive to decision-making, defining and resolving action items, issuing agendas and meeting minutes, and maintaining project document repository to ensure transparency across the team
May be requested to provide oversight of the PMO or oversight of PMO initiatives as needed
Responsible as a key contact for program team related information and for obtaining and maintaining a comprehensive knowledge of the program scope, deliverables, timelines, status and key risks and mitigation strategies
SK Life Science Labs Support :
Manage critical components of specific compound-based projects as assigned
Assist Finance team with implementation and maintenance of Purchase Order Management
Support organizational budget management, as requested
Manage ad-hoc projects as assigned
Qualifications :
A Bachelor's Degree with an Advanced Degree in relevant field strongly preferred; PMI PMP Certification preferred
10-15+ years of Project Management experience
Drug discovery and development knowledge across a broad range of functions and therapeutic areas
Knowledge of relevant pharmaceutical quality and regulatory standards requirements
Proven track record of project and / or operational support for successful IND, CTA, NDA, and / or BLA regulatory submissions
Track record of creating strategies, long-term planning and managing integrated timelines and resources
Intellectual agility - able to pivot based on shifting priorities and balance multiple projects seamlessly in a fast-paced environment
Ability to multitask
Adapts to change
Maintains composure under pressure
Ability to follow verbal or written instructions and use of effective verbal communications
Adapts change, adjust change and grasps information quickly
Examine and observe details
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.