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ICON plc

Senior Principal Biostatistician

ICON plc

. Lead statistical methodologies and contribute to the design and analysis of clinical studies .

Posted 9/15/2026full-timeRemote • United KingdomSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Expertise in biostatistics and statistical methodologies, with a strong focus on clinical trial design, data analysis, and regulatory compliance. Proven ability to lead teams, mentor junior statisticians, and communicate complex statistical concepts effectively.

Highest-signal resume keywords
BiostatisticsClinical Trial DesignStatistical Analysis PlansSASR

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Statistical MethodologiesData AnalysisClinical Study DesignStatistical Software ProficiencyRegulatory Submissions
Soft Skills
Problem-SolvingLeadershipCommunicationDetail-OrientedOrganizational Skills
Industry Keywords
Pharmaceutical IndustryBiotech IndustryClinical TrialsData ManagementRegulatory Guidelines

About the role

Key responsibilities & impact
  • Lead statistical methodologies and contribute to the design and analysis of clinical studies
  • Oversee biostatistics workstreams, ensuring deliverables meet quality and timeline expectations
  • Design and implement statistical analysis plans for clinical trials, aligned with study objectives and regulatory guidelines
  • Oversee statistical analysis of clinical data and provide insights and interpretations for decision-making and reporting
  • Collaborate with clinical, regulatory, and data management teams
  • Mentor junior statisticians and provide training on statistical methodologies and software applications
  • Contribute to regulatory submissions and publications
  • Stay updated on industry trends and advancements in statistical methodologies
  • Participate in protocol development and provide input on endpoints and statistical considerations

Requirements

What you’ll need
  • A master's degree or Ph.D. in Biostatistics, Statistics, or a related field
  • Extensive experience in biostatistics within the pharmaceutical or biotech industry, particularly in clinical trial design and analysis
  • Strong knowledge of statistical software (e.g., SAS, R) and proficiency in programming for data analysis
  • Excellent problem-solving skills, with the ability to interpret complex data and provide actionable insights
  • Demonstrated leadership abilities, with experience in mentoring and guiding teams
  • Strong communication skills, with the ability to present statistical concepts to non-statistical audiences effectively
  • Detail-oriented, with excellent organizational skills to manage multiple projects and meet deadlines in a fast-paced environment
  • Legal right to work in the country where the role is based

Benefits

Comp & perks
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways