Principal Biostatistician

Precision Medicine Group; Greater London; Sur place; GBP 90 000 - 140 000; Plein temps

Résumé du poste

Precision Medicine Group is seeking a senior biostatistician to provide expert statistical support across the clinical development lifecycle in the UK. You will write and review statistical sections of protocols, develop SAS programs for listings and tables, and lead complex study designs in collaboration with sponsors and project teams.

The role requires a Master’s in Statistics or Biostatistics (PhD preferred) and 10+ years of industry experience, with strong knowledge of ICH, CDISC, and

Qualifications

• 10+ years of experience in statistics/biostatistics within clinical development.
• Experience writing SDTM/ADaM datasets and statistical analysis plans.
• Ability to work with sponsors and cross-functional teams.

Responsabilités

• Develop and review statistical methods for clinical study protocols including complex designs.
• Author and review statistical analysis plans for late-phase studies.
• Produce tables, listings, and figures from SAS datasets for reports and submissions.
• Provide statistical support to Data Monitoring Committees and project teams.

Connaissances

SAS programming

Statistical methods

Communication

Project leadership

Data analysis

Formation

Master's degree in Statistics/Biostatistics

PhD in Statistics/Biostatistics

Outils

SAS

CDISC

Description du poste

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:

• 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:

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

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 andtechniques

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 organizational skills, time management, and ability to coordinate workloadand meet established deadlines.
• Excellent communication and interpersonal skills to effectively interface with others.
• Excellent problem-solving skills
• Excellent presentation skills
• 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

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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 [e-mail] .

Candidates must be legally authorized to work in the country of employment without employer sponsorship.