Senior Statistician II, Late Oncology
AstraZeneca Voir toutes les offres
- Mississauga, ON
- 109.149-143.258 $ par an
- Contrat
- Temps-plein
- Offer statistical support for planning experimental work and clinical studies. Build clear decision criteria and power plans to address the right questions with relevant evidence.
- With mentorship from experienced statisticians, lead the development and analysis of complex studies. Support broader programs including preclinical investigations, regulatory submissions, commercialization activities, and interactions with senior governance bodies.
- Simulation and modelling: Apply simulation and modelling to inform study build decisions, assess robustness and operating characteristics, and examine scenarios under pressure to minimize risks in development plans.
- Analysis Planning and Execution: Develop Statistical Analysis Plans; produce analyses, graphics and tables for standard studies and reports across clinical, preclinical, medical affairs and publication needs with accuracy and timeliness.
- Insightful Interpretation and Communication: Interpret, summarize and communicate findings from standard studies in a way that influences decisions and next steps, translating statistics into clear, actionable mentorship.
- Methodology and Process Improvement: Contribute to improved methods and practical solutions that raise quality, efficiency and effectiveness; embed best practices in how we plan, execute and report studies.
- Manage your work to meet deadlines and standards. Be accountable for your statistical deliverables' integrity. Provide discipline-specific insight and constructive challenge. Recognize your own development needs.
- Provides statistical expertise to build studies and to evaluate and interpret experimental results in research projects and clinical trials. Refers to more senior statistical experts when necessary.
- Leads own work to schedule and quality and applies a range of statistical methods
- Demonstrates independence in delivering statistical assistance for standard building and interpretation of study data
- Under the mentorship of a more experienced statistician, composes and analyzes complex studies. Provides statistical help for broader programs, including preclinical studies, regulatory submissions, commercialization efforts, or internal governance committee interactions.
- Under mentorship of a statistician with greater expertise, analyzes internal and external information to inform building decisions and the development of decision criteria
- Applies modelling and simulation to inform study design and assess robustness of results
- Develops a Statistical Analysis Plan for study and/or project delivery
- Produces analysis, supporting graphics and data tables for routine studies, such as in preclinical or clinical study reports, Global Medical Affairs studies or publications
- Interprets, summarizes and communicates results of standard studies
- Plays a role in improving methodology and offers practical solutions for problems
- Applies statistical methodology to improve process and delivery activities
- Contributes to crafting guidelines to improve quality, efficiency and effectiveness
- Accountable for the quality of statistical work; provides discipline-specific understanding, perspective and thoughtful critique and is self-aware of own development needs
- Able to solve complex problems within own area and participates in multidisciplinary teams
- Experience in late-stage oncology trials along with knowledge of disease endpoints and estimands
- Proficiency in SAS and R, with experience in reproducible workflows and version control
- Familiarity with regulatory guidelines and submissions, including ICH E9 and related addenda
- Experience with Bayesian or simulation-based design approaches and decision frameworks
- Strong communication skills to influence non-statistical partners and present at governance forums
- Record of contributions to publications or conference presentations