Disclaimer: Hunt UK Visa Sponsors aggregates job listings from publicly available sources, such as search engines, to assist with your job hunting. We do not claim affiliation with Medpace. For the most up-to-date job details, please visit the official website by clicking "Apply Now."
Due to continuous business growth, we are expanding our Global Biostatistics team, and looking for an experienced Statistical Analyst to join our UK team in London, Stirling or home-based.
This role is responsible for leading the Biostatistics activities for multiple complex clinical trial projects, working directly with the client and collaborating with other departments and Clinical Trial Management team, operating in a leadership position and representing the Biostatistics department at client meetings.
This position will work in 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
- Development of detailed Medpace Data Analysis Plan for assigned projects;
- Development of analysis databases;
- Communication of project requirements for CRF design, database design, and database clean-up to ensure the key study variables are suitable for analysis;
- Programming of study analysis, review of study results, and preparation of statistical methods section for clinical/statistical reports, and related regulatory submission documents;
- Communication of statistical results to medical writing personnel to ensure accurate interpretation; and
- Collaboration with Global Statistics team members and programmers to ensure study outputs are produced to a high quality and in a timely fashion.
Qualifications
- Master’s Degree in statistics, biostatistics, or equivalent areas and strong relevant industry or equivalent experience;
- SAS Programming experience;
- Excellent communication and leadership skills;
- Familiarity with regulatory requirements/guidelines for data submission and analysis;
- Expertise in biostatistical methodologies applicable to Clinical Trials; and
- Knowledge of advanced programming methods.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide 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. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Awards
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What To Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
