Biostatistician – Clinical Trials with On-site Mentors

Medpace, Inc.

Stirling

On-site

GBP 60,000 - 90,000

Full time

14 days+

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Benefits offered by this job

On-site mentors

Career paths and advancement

Industry onboarding and training

WFH flexibility after training

Company-sponsored events

Job summary

Medpace, Inc. is seeking a full-time Biostatistician to join our office-based team in Central London or Stirling. You will collaborate within a biostatistics group to support clinical trial projects, ensuring timely delivery and high quality work.

Responsibilities include protocol review, data analysis plan development, programming analyses, and communicating results to medical writing. A PhD in Biostatistics or related field and SAS programming experience are required; pharma or CRO background

Qualifications

PhD in Biostatistics or related field.
Experience with SAS programming.
Knowledge of advanced statistical methods used in clinical trials.
Familiarity with regulatory guidelines for drug development.
Pharma/CRO experience preferred.

Responsibilities

Contribute to biostatistics activities for clinical trial projects.
Review study protocols and develop statistical methodologies.
Develop detailed Data Analysis Plans for projects.
Program analyses, review results, and prepare statistical sections for reports.
Communicate CRF design, database design, and data cleanup requirements for analysis.
Present statistical results to medical writing personnel for interpretation.