Create, maintain, and manage integrated study schedules in Microsoft Project including key events, roadmaps, and critical-path visualizations.
Identify opportunities to accelerate development timelines while maintaining quality and compliance.
Leverage digital planning platforms, integrated timelines, predictive analytics, dashboards, and program management tools to improve predictability and execution.
Align clinical trial timelines with integrated clinical and compound development plans.
Develop budget, timeline, and FTE forecasts; create scenario analyses in Planisware to support decision‑making.
Identify and proactively manage risks, issues, assumptions, decisions, and dependencies.
Collect, consolidate, and report financial, timeline, and resource metrics for governance reviews and external funding partnerships.
Maintain study governance documentation, After Action Review and lessons learned.
Support governance reviews, investment decisions, and portfolio prioritization activities.
Requirements
Minimum of a Bachelor's degree in Life Sciences, Nursing, Pharmacy, Business, or related discipline is required.
Minimum 8 years of experience in pharmaceutical, healthcare, biotechnology, or related industries.
Demonstrated experience leading complex clinical development programs.
Knowledge of project management methodologies, systems, and tools.
Demonstrated expertise in MS Project.
Proficiency with technology enabling tools including Visio, Excel, etc.
Experience mentoring/coaching others.
Experience operating in matrixed global organizations and leading without authority.
Demonstrated ability to be creative and flexible to change/improve working environment in broad context.
Preferred: Professional project management certification (i.e., PMP, CPM, etc.)