Principal Biostatistician

Job title:

Principal Biostatistician

Company

Atorus

Job description

Principal Biostatistician
Remote from the U.S. or Canada
Full-time or Contract (candidate’s preference)JOB OVERVIEW
The Principal Biostatistician is responsible for the departmental efforts in developing and implementing innovative statistical methods in accordance with Atorus and/or sponsor standard operating procedures (SOPs), Good Clinical Practice (GCP), ICH Guidelines and sponsor requirements. Additional responsibilities include providing leadership and statistical/strategic input to the clinical development plans and being a key contributor to clinical protocols for statistical concepts as well as broader drug development concepts.RESPONSIBILITIES

• Perform/oversee the analysis of clinical trial data, provide statistical interpretation of results, and collaborate on the reporting of clinical trial results to Sponsor, regulatory authorities, and the scientific community.
• Provide oversight of statistical analysis plans, statistical outputs, and other documents as required.
• Represent company and the statistical team on the Product Development Teams of sponsors.
• Provide statistical and methodological consultation on special statistical methodology or statistical, scientific, and regulatory issues.
• Collaborate with medical monitors and other study personnel on the creation of clinical trial designs.
• Perform or oversee power/sample size calculations to determine appropriate trial size; run simulations to assess operating characteristics of a design.
• Provide statistically sound experimental design and data analysis inputs to meet project objectives and regulatory requirements.
• Work with medical monitors to develop ad hoc analysis plans and ensure analyses are performed appropriately by statistical programmers.
• Keeps abreast of new developments in statistics, drug development, and regulatory guidance through literature review and attendance at workshops and professional meetings.
• Key contributor in project planning.
• Develop strong collaboration and communication with sponsor cross-functional teams and sponsor Biostatistics management.
• Manage biostatisticians and statistical programmers with respect to statistical strategy, deliverables and processes.
• Develop and assist in maintenance of department tools, templates, guidelines, SOPs, and systems.

QUALIFICATIONS AND EDUCATION REQUIREMENTS

• Master’s degree in Statistics, Biostatistics, or related discipline. Ph.D. preferred.
• 10+ with Master’s/7+ with PhD years’ experience in statistical or biostatistical analysis supporting clinical trial operations for drug development in the pharma/biotech industry
• Proficiency working knowledge of SAS and/or R programming languages
• Study Lead experience working with cross-functional teams. Experience leading global teams a plus.
• Experience in sample size calculation, protocol concept development, protocol development, SAP and preparing clinical study reports including integrated summaries for submissions.
• Good SAS programming skills for QCing critical outputs, Efficacy/Safety tables and working closely with Programmers. Knowledge of R programming a plus.
• Solid understanding & implementation of CDISC requirement for regulatory submissions.
• Adept in ADaM specifications generation and review of datasets.
• Effective communicator: able to explain methodology and consequences of decisions in lay terms.
• In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Familiarity with advanced, complex statistical methods that apply to applicable clinical trials.
• Knowledge of FDA regulations, ICH GCP guidelines, the drug development process

Expected salary

Location

Canada

Job date

Thu, 24 Oct 2024 01:25:47 GMT

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