Biostatistician II

Parexel

. Contribute to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions .

Posted 11/11/2026full-timeRemote • United KingdomMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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

Demonstrates expertise in statistical analysis and programming, particularly in SAS and R, with a strong understanding of clinical trial methodologies. Capable of leading project teams, providing statistical advice, and ensuring high-quality outputs in a client-focused environment.

Highest-signal resume keywords

SAS ProgrammingR ProgrammingStatistical AnalysisClinical Trials ExpertiseLeadership Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical MethodsData Quality ControlAnalysis PlansStatistical ReportsDerived Datasets

Soft Skills

ConfidenceSelf-RelianceStrong Communication SkillsWork Ethic

Certifications & Qualifications

Master's Degree in StatisticsPhD in Statistics

Industry Keywords

Clinical TrialsObservational StudiesRegulatory SubmissionsStatistical OutputsProcess Improvement

About the role

Key responsibilities & impact

Contribute to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions
Independently program and quality-control derived datasets and statistical outputs, including tables, listings, and figures
Produce analysis plans and reports under the supervision of an experienced biostatistician
Provide basic statistical advice to clients
Produce and/or QC derived datasets and simple and advanced statistical outputs using efficient programming techniques
Understand and apply moderately advanced statistical methods
Coordinate and lead project teams to complete projects within timelines and budget
Interact with clients as a key contact regarding statistical and contractual issues
Assist with analysis plans, statistical reports, statistical sections of integrated clinical reports, and process-supporting documents
Check work on an ongoing basis to ensure first-time quality
Provide training in statistical analysis to internal clients
Participate in or lead process and quality improvement initiatives
Travel to, attend, and contribute to client meetings, including discussing analysis concepts and presenting study results

Requirements

What you’ll need

Master's Degree in Statistics plus a minimum of 3 years industry experience OR PhD in Statistics plus 1 year of industry related experience
Thorough understanding of the statistical aspects of clinical trials and/or observational studies
Experience in statistical analysis in a clinically related subject, within clinical trials
SAS programming or R programming skills
Confidence, self-reliance, and ability to learn quickly in a matrixed team
Good leadership skills
Strong oral and written English communication skills
Strong work ethic to promote the development of life-changing treatments for patients

Benefits

Comp & perks

Virtual resources supporting collaborative and effective work across the globe
Opportunities to work collaboratively with colleagues across the globe
Training in statistical analysis for internal clients
Participation in process and quality improvement initiatives