Novartis is looking to solve the problem of implementing modern and innovative trial/experimental designs, statistical models, and analysis and data exploration methodologies at the study or project level in late phase drug development.
Requirements
- PhD with 3+ years experience or MS with 7+ years preferred.
- Strong knowledge of biostatistics and statistical analysis.
- Experience with automation, computer programming, and metadata management.
- Experience with clinical trials and statistical consultation.
- Strong understanding of statistical models and data exploration methodologies.
- Experience with innovative trial designs and novel methods.
- Strong programming skills
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.
Other
- Fluent English (oral and written).
- Strong communication and presentation skills.
- Ability to work collaboratively in a cross-functional team.
- Ability to drive quantitative decision making in assigned indications/program.
- Ability to work with consultants, advisory boards, health authorities, congresses, and scientific meetings.
