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For Companies At a Glance
- Tasks: Lead biostatistics for complex clinical trials and collaborate with various teams.
- Company: Medpace is a global CRO dedicated to advancing medical therapeutics.
- Benefits: Enjoy flexible work, competitive pay, and structured career growth opportunities.
- Why this job: Make a real impact on patients' lives while developing your expertise in a supportive environment.
- Qualifications: Master's in statistics or biostatistics, SAS experience, and strong communication skills required.
- Other info: Join a company recognised by Forbes for its success and commitment to quality.
The predicted salary is between 43200 - 72000 £ per year.
Overview
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 the 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.
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Statistical Analyst (Experienced, SAS) - London employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Statistical Analyst (Experienced, SAS) - London
✨Tip Number 1
Familiarise yourself with the latest biostatistical methodologies and SAS programming techniques. This will not only boost your confidence but also demonstrate your commitment to staying current in the field during interviews.
✨Tip Number 2
Network with professionals in the clinical trial and biostatistics sectors. Attend relevant conferences or webinars, and connect with people on platforms like LinkedIn to gain insights and potentially get referrals for the role.
✨Tip Number 3
Prepare to discuss specific projects where you led biostatistical activities. Highlight your leadership skills and how you effectively communicated results to various stakeholders, as this is crucial for the role.
✨Tip Number 4
Research Medpace’s recent projects and achievements in the clinical research field. Being knowledgeable about the company will help you tailor your conversation and show genuine interest during the interview process.
We think you need these skills to ace Statistical Analyst (Experienced, SAS) - London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience with SAS programming and biostatistics. Emphasise any relevant projects or roles that demonstrate your leadership skills and ability to work on complex clinical trials.
Craft a Compelling Cover Letter: Write a cover letter that specifically addresses the responsibilities mentioned in the job description. Discuss your previous experience in developing data analysis plans and collaborating with cross-functional teams, showcasing how you can contribute to Medpace's success.
Highlight Relevant Qualifications: In your application, clearly state your Master's Degree in statistics or biostatistics and any additional certifications. Mention your familiarity with regulatory requirements and advanced programming methods, as these are crucial for the role.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or typos. A polished application reflects your attention to detail, which is essential for a Statistical Analyst position.
How to prepare for a job interview at Medpace
✨Showcase Your SAS Skills
Since the role requires strong SAS programming experience, be prepared to discuss specific projects where you've used SAS. Highlight any complex analyses you've conducted and how they contributed to the success of your previous teams.
✨Demonstrate Leadership Experience
As this position involves a leadership role, share examples of how you've led teams or projects in the past. Discuss your approach to collaboration and how you ensure high-quality outputs while meeting deadlines.
✨Understand Regulatory Requirements
Familiarise yourself with the regulatory guidelines relevant to clinical trials. Be ready to discuss how you've navigated these requirements in your previous roles and how you ensure compliance in your work.
✨Prepare for Technical Questions
Expect technical questions related to biostatistical methodologies and data analysis plans. Brush up on key concepts and be ready to explain your thought process when developing analysis databases or communicating project requirements.
