Principal Biostatistician
LocationLondon
Posted2 hours ago
Position Summary:
Job Description
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 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)
Skills:
Mastery of statistical principles underlying clinical trials
Mastery of SAS programming skills and familiarity with other packages
Outstanding statistical skills
Excellent consultative skills
Excellent organizational skills, time management, and ability to coordinate workload and meet established deadlines.
Excellent communication and interpersonal skills to effectively interface with others.
Excellent problem-solving skills
Excellent presentation skills
Competencies:
Sound judgment/decision making
Ability to establish and teach others to maintain effective working relationships with coworkers, managers and clients
Service oriented, accountable and flexible
Competency in written and spoken English
Follow and train others on applicable regulations, including FDA, ICH, and Precision Policies and Procedures
Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at
Job Description
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 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)
Skills:
Mastery of statistical principles underlying clinical trials
Mastery of SAS programming skills and familiarity with other packages
Outstanding statistical skills
Excellent consultative skills
Excellent organizational skills, time management, and ability to coordinate workload and meet established deadlines.
Excellent communication and interpersonal skills to effectively interface with others.
Excellent problem-solving skills
Excellent presentation skills
Competencies:
Sound judgment/decision making
Ability to establish and teach others to maintain effective working relationships with coworkers, managers and clients
Service oriented, accountable and flexible
Competency in written and spoken English
Follow and train others on applicable regulations, including FDA, ICH, and Precision Policies and Procedures
Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at
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