Biostatistician

Medpace; Lyon; On-site; EUR 45,000 - 70,000; Full time

Job summary

An established industry player is seeking a dedicated Biostatistician to join their dynamic team in Lyon. This full-time, office-based role offers the chance to contribute significantly to clinical development projects, utilizing your expertise in statistical methodologies and SAS programming. You will play a vital role in preparing study analyses, reviewing results, and ensuring accurate communication of statistical findings to enhance project success. If you are passionate about making a difference in the clinical research field and eager to grow your career, this opportunity is perfect for you.

Qualifications

• Ph.D. in Biostatistics/Statistics required.
• 1-2 years experience in a pharmaceutical or CRO setting preferred.

Responsibilities

• Contribute to clinical development of plan preparation.
• Review study protocol and prepare statistical methodologies.
• Communicate statistical results to ensure accurate interpretation.

Skills

SAS Programming

Statistical Analysis

Clinical Development

Communication

Education

Ph.D. in Biostatistics/Statistics

Tools

Statistical Software

Job description

Job Summary

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Biostatistician to join our team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can 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;
• 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 cleanup to ensure the key study variables are suitable for analysis;
• Communicate statistical results to medical writing personnel to ensure accurate interpretation.

Qualifications

• Ph.D. degree in Biostatistics/Statistics with strong experience in SAS Programming or equivalent;
• 1-2 years of experience in a pharmaceutical or CRO setting preferred.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV 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 its scientific and disciplined approach.