Vacancy expired!
- Partner with the Development Program Lead (DPL) to lead a cross-functional matrix team of experts in advancing a Centessa clinical asset within the remit of their Development Program Team (DPT).
- Design, implement, and monitor integrated multidisciplinary development project plans that enable the strategy, allow for data driven decision making, and ensure alignment on timeline, budget, scope, and deliverables
- Pro-actively identify program risks and mitigation strategies
- Maintain project dashboards, Gantt charts, finance systems, and documents to track and report on progress
- Drive efficient decision making by acting as a key liaison between the project team and stakeholders while effectively communicating project status and progress to management, partners, and governance teams
- Manage interdependencies and connections between functions and ensure visibility and alignment
- Facilitate cross-functional team meetings in preparing agendas, presentation materials, and meeting minutes that ensure follow up of action items
- Provide periodic status reports regarding study timelines, accruals, etc. as requested
- Provide support for the planning and preparation of documents to a quality standard required for Regulatory/Health Authority submissions
- Work effectively in a global and virtual environment with an international team, operating across US, EU, and Asia time zones
- 4+ years' experience in the life sciences industry, with 2+ years of Project Management experience in clinical drug or program development or equivalent academic experience in clinical trials.
- MUST have experience with natural history, or an interest on working on a natural history study
- Strong communication, collaboration, interpersonal skills, and influence to accomplish work without formal authority and to ensure optimal team performance.
- Ability to work collaboratively with others within and external to the company, including investigators, CROs, vendors and global team members.
- Excellent analytical and organizational skills (resources, timelines, cost/risk/benefit analysis, and overseeing data management)
- Working knowledge of project management principles and practices with the ability to thrive in a fast-paced versatile environment (PMP certification is an advantage)
- Familiarity with the design and conduct of clinical trials and project management in company relevant therapeutic areas
- Working knowledge of current global regulatory requirements and guidelines for clinical trials
Vacancy expired!