Responsibilities:
- Responsible for all statistical tasks on assigned trials.
- Contribute to protocol development, develop the statistical analysis plan, and support reporting activities.
- Plan and execute exploratory analyses and provide statistical consultation within cross-functional teams.
- Initiate, drive, and implement novel methods and innovative trial designs (aligned with the Lead Statistician).
- Collaborate with clinical, regulatory, and strategic functions to drive quantitative decision-making for assigned indications/programs (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.
Qualifications / Required Skills:
- PhD with 3+ yearsβ experience (preferred) OR MS with 7+ yearsβ experience; Principal/Senior Principal level commensurate with experience.
- Fluent English (oral and written).
- Strong communication and presentation skills.
Compensation & Benefits (if stated):
- Salary range expected: $119,700β$222,300/year; may include performance-based cash incentive and possible annual equity awards; comprehensive benefits (health, life, disability, 401(k) match/contribution, time off).
Application / Accessibility instruction (if needed):
- For reasonable accommodations, email tas.nacomms@novartis.com or call +1(877)395-2339; include the job requisition number.
Location:
- Onsite, East Hanover, NJ (not available for remote work).