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Virtual Statistics Recruitment Event - London & Stirling - Job Opportunity at Medpace, Inc.

London & Stirling, United Kingdom
Full-time
Entry-level to Senior
Posted: April 19, 2025
On-site
GBP 35,000-90,000 annually depending on role level and experience, with Statistical Analysts at the lower end and PhD Biostatisticians at the upper end

Benefits

Global career development opportunities
Opportunity to work on cutting-edge clinical trials
Career advancement in a growing CRO
Professional development in biostatistics
Work with diverse therapeutic areas

Key Responsibilities

Design and implement statistical analyses for clinical trials
Develop and validate SAS programming for clinical data analysis
Collaborate with cross-functional teams on study design
Contribute to statistical methodology development
Ensure data quality and integrity in clinical trials
Prepare statistical documentation for regulatory submissions

Requirements

Education

BS, MS or PhD in Statistics or related field

Required Skills

SAS Programming Statistical analysis Clinical trial methodology Database management Communication skills Project coordination
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Industry Trends

The biostatistics field is experiencing rapid growth due to increasing complexity in clinical trials and regulatory requirements Integration of advanced analytics and machine learning with traditional statistical methods is becoming more common Rising demand for real-world evidence analysis is creating new opportunities in the CRO sector Increasing focus on adaptive trial designs and innovative statistical methodologies

Role Significance

Typically part of a 5-15 person biostatistics team within larger clinical operations structure
Multiple levels available from entry-level Statistical Analyst to senior Biostatistician positions, offering clear career progression paths

Key Projects

Phase I-IV clinical trials across multiple therapeutic areas Regulatory submission support Statistical methodology development Real-world evidence analysis

Success Factors

Strong foundation in statistical theory and practical application Ability to translate complex statistical concepts for non-technical stakeholders Attention to detail and quality in regulatory environments Effective collaboration with cross-functional teams

Market Demand

High demand with projected growth due to increasing complexity in clinical trials and expanding pharmaceutical research

Important Skills

Critical Skills

SAS programming expertise is fundamental for data analysis and reporting Statistical methodology knowledge for trial design and analysis Communication skills for cross-functional collaboration Understanding of regulatory requirements in clinical trials

Beneficial Skills

R or Python programming Experience with adaptive trial designs Knowledge of machine learning applications in clinical research Understanding of CDISC standards

Unique Aspects

Opportunity to work across multiple therapeutic areas
Exposure to various phases of clinical development
Strong focus on statistical methodology innovation
Clear career progression path within a growing organization

Career Growth

Typical progression from Statistical Analyst to Biostatistician in 3-5 years with appropriate education and performance

Potential Next Roles

Senior Biostatistician Statistical Programming Manager Director of Biostatistics Head of Clinical Development

Company Overview

Medpace, Inc.

Medpace is a well-established mid-sized CRO with a strong focus on full-service clinical research support across all major therapeutic areas

Among top 10 global CROs with strong reputation for quality and scientific expertise
Strategic expansion in UK market with dual locations in London and Stirling showing commitment to growth
Professional environment with emphasis on scientific rigor and career development
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