At a Glance
- Tasks: Lead biostatistics activities for complex clinical trials and collaborate with various teams.
- Company: Join a growing global biostatistics team in a flexible work environment.
- Benefits: Enjoy competitive pay, flexible hours, and great career growth opportunities.
- Other info: Participate in employee appreciation events and wellness initiatives.
- Why this job: Make a real impact in clinical trials while developing your statistical expertise.
- Qualifications: Master’s in statistics or biostatistics, SAS programming experience, and strong communication skills.
The predicted salary is between 50000 - 65000 € per year.
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;
- 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;
- Knowledge of advanced programming methods.
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
Statistical Analyst (Experienced, SAS) - London employer: Medpace, Inc.
Medpace is an exceptional employer that fosters a flexible work environment and prioritises employee well-being through health initiatives and competitive benefits. With structured career paths and opportunities for professional growth, our London-based team thrives on collaboration and innovation, making it an ideal place for experienced Statistical Analysts to advance their careers while contributing to impactful clinical trial projects.
StudySmarter Expert Advice🤫
We think this is how you could land Statistical Analyst (Experienced, SAS) - London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know that can land you that dream job.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to statistical analysis and clinical trials. We recommend doing mock interviews with friends or mentors to boost your confidence and refine your answers.
✨Tip Number 3
Showcase your skills! Create a portfolio of your previous work, especially any SAS programming projects or biostatistical analyses you've done. This will give potential employers a tangible sense of your expertise and how you can contribute to their team.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who are proactive and engaged with our company.
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 is tailored to the Statistical Analyst role. Highlight your SAS programming experience and any relevant biostatistical methodologies you've used in previous projects. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about biostatistics and how your experience aligns with our needs. Don’t forget to mention your leadership skills and how you can contribute to our team.
Showcase Your Communication Skills:Since this role involves collaboration with various teams, make sure to highlight your communication skills in your application. We love candidates who can clearly convey complex statistical concepts to non-technical stakeholders!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the details about the role and our company culture there!
How to prepare for a job interview at Medpace, Inc.
✨Know Your SAS Inside Out
Make sure you brush up on your SAS programming skills before the interview. Be prepared to discuss specific projects where you've used SAS, and think about how you can demonstrate your expertise in biostatistical methodologies relevant to clinical trials.
✨Showcase Your Leadership Skills
Since this role involves leading Biostatistics activities, be ready to share examples of how you've successfully led teams or projects in the past. Highlight your communication skills and how you've collaborated with other departments to achieve project goals.
✨Understand the Regulatory Landscape
Familiarise yourself with the regulatory requirements and guidelines for data submission and analysis. Being able to discuss these in the context of your previous work will show that you’re not just technically skilled but also aware of the bigger picture in clinical trials.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare thoughtful questions about the company’s approach to biostatistics, team dynamics, and opportunities for professional growth. This shows your genuine interest in the role and helps you assess if it’s the right fit for you.
