Your Key Responsibilities:

• Responsible for all statistical tasks on the assigned trials.
• Protocol development in alignment with the development plan, developing statistical analysis plan, reporting activities.
• Contribute to planning and execution of statistical analyses and statistical consultation within your cross-functional teams.
• Initiate, drive and implement novel methods and innovative trial designs in alignment with the Lead Statistician.
• Collaborate with clinical, regulatory and other strategic functions to drive quantitative decision making in assigned indications/program with oversight.
• Collaborate cross-functionally (e.g. data management, programming, medical writing) to ensure timeliness and quality of statistical deliverables.
• Contribute to external engagement with consultants, advisory boards, health authorities, congresses, and scientific meetings
  

Role Requirements:
Essential Requirements:

• PhD with 3+ years’ experience preferred OR MS with 7+ years’ experience
• Fluent English (oral and written)
• Strong communication and presentation skills