Biostatistician

Medpace, Inc.; Stirling; On-site; GBP 60,000 - 90,000; Full time

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.

Skills

PhD in Biostatistics/Statistics/Med.统计

SAS Programming

Advanced statistical methods

Regulatory knowledge (drug development

Pharma/CRO experience preferred

Education

Ph.D. in Biostatistics / Statistics / Medical Statistics

Tools

SAS Programming

Job description

Job Summary

Due to continuous business growth, we are expanding our Biostatistics team, and looking for a full-time Biostatistician to join our office-based team in Central London or Stirling. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success.

This role is responsible for Biostatistics activities for clinical trial projects; to ensure that work is completed within the defined time frames to appropriate quality levels, and present the Biostatistics function at conferences, external non-study meetings and bid defense meetings. If you want an exciting career where you can use your previous expertise and develop and grow your career even further, then this is the opportunity for you.

Responsibilities

• Contribute to clinical development of plan preparation;
• Review of study protocol and preparation of statistical methodologies;
• Development of detailed Data Analysis Plan for assigned projects;
• Programming of study analysis, review of study results and preparation of statistical methods section for clinical / statistical reports;
• Communicate project requirements for CRF design, database design and database clean-up to ensure the key study variables are suitable for analysis; and
• Communicate statistical results to medical writing personnel to ensure accurate interpretation.

Qualifications

• Ph.D. degree in Biostatistics / Statistics / Medical Statistics;
• Experience in SAS Programming;
• Knowledge of advanced statistical methods and knowledge of the pharmaceutical industry;
• Knowledge of regulatory requirements/guidelines for drug development; and
• Previous experience in a pharmaceutical or CRO preferred.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

• Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
• Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

• Office based environment with on-site mentors
• Defined career paths with clear advancement opportunities
• Industry renowned onboarding and training programs designed to accelerate professional development
• Ongoing training and continuous learning opportunities throughout your career
• An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

• Competitive compensation programs that recognize and reward performance
• Comprehensive health, wellness, retirement, and PTO benefits
• Office based culture with occasional WFH that provides flexibility for eligible positions after training
• Company-sponsored social events

Please note benefits may vary based on country.