Job Application for Principal Biostatistician (Oncology - Clinical Trials) at Precision Medicine Group

***This is a 100% remote opportunity in the US or Canada.***

***Unfortunately, we are not able to work with anyone on sponsorship or requiring a visa sponsorship now or anytime in the future.***

Principal Biostatistician

Provides statistical support for all phases of clinical development. Specific responsibilities include writing and reviewing statistical sections of protocols, writing and reviewing statistical analysis plans including complex study designs, conducting statistical analyses and presenting results to project teams and sponsors, and developing SAS programs for tables, listings, figures and analysis datasets in accordance with Precision and/or sponsor procedures or study specific guidelines.

Essential functions of the job include but are not limited to:

Generate and/or verify randomization schedules
Develop and review statistical methods of the clinical study protocol including complex study designs
Provide and/or verify sample size calculations. Perform or assist with advanced calculations including adaptive design
Provide input into development of case report forms (CRFs)
Author statistical analysis plans, including development of table, figure and listing shells, complex study design and late phase
Review statistical analysis plans written by other biostatisticians
Generate analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS
Perform quality control for statistical based SAS programs and other study documents (e.g., presentations and reports)
Provide or supervise programming and statistical support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests
Ability to serve as a biostatistical consultant to company staff globally, with understanding of varying regional perspectives
Review output across programs to ensure consistency.
Provide statistical analysis and reports to Data Monitoring Committees (DMCs) as the unblinded biostatistician
Review statistical sections of clinical study reports
Work directly with sponsors, project managers, and external vendors on statistics[1]related project components
Interact directly with study team
Interact directly with sponsors
Lead all statistical activities for study within timelines
Independently perform budget health review on projects and review monthly invoices
Perform oversight responsibilities on projects for other biostatisticians
Assist with budget development and present at bid defense meetings
Participate in the development and maintenance of departmental procedures and standards (templates, SOPs, WIs etc.)
Review study tasks to ensure study being conducted in line with agreed budget; identify change in scope
Other duties as assigned

Qualifications:

Minimum Required:

Master's degree or equivalent in Statistics, Biostatistics, or related field with 10+ years experience; PhD degree in Statistics, Biostatistics, or related field with 7+ years experience

Other Required:

Experience with SAS
Knowledge of industry standards such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines
Broad knowledge and superior understanding of advanced statistical concepts and techniques Preferred:
Experience with Oncology and rare diseases
Broad experience with late phase and/or submissions
Experience in consulting with clients on study design
Superior understanding of a specific therapeutic area and/or statistical methodology (eg, adaptive design, missing data

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Principal Biostatistician (Oncology - Clinical Trials)

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