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- Tasks: Lead statistical activities for global clinical trials and collaborate with international teams.
- Company: Top-tier CRO dedicated to excellence in clinical research.
- Benefits: Competitive salary, flexible work options, and opportunities for professional growth.
- Why this job: Make a real impact in clinical research while working with expert teams.
- Qualifications: MSc in Statistics and expertise in SAS programming and clinical research standards.
- Other info: Join a dynamic team focused on innovation and quality in clinical trials.
The predicted salary is between 48000 - 72000 £ per year.
Overview
You will contribute to statistical activities related to global clinical trials and work closely with international teams of statisticians, programmers and data managers, including the role of biostatistics project lead.
Responsibilities
- Act as a communication line for project teams, clients, vendors and internal team on statistical questions
- Conduct statistical analysis for clinical trials including interim analysis, final analysis, analysis for DSMBs/DMCs and PK analysis
- Develop and review study protocols, statistical analysis plans, analysis dataset specifications according to CDISC ADaM standard and other project-specific documents
- Review statistical deliverables such as tables, figures, listings and analysis datasets
- Conduct departmental induction course and project-specific training for statisticians and SAS programmers
- Prepare for and attend internal and external study audits pertinent to Statistics
- Participate in preparation of internal/external audits follow up
- Provide input to standard operating procedures and other Quality Systems Documents (QSDs) pertinent to activities of Biostatistics department
- Liaise with DM on statistical questions related to data issues
- Participate in bid defense and in kick-off meetings
- Lead teams of SAS programmers and/or statisticians on the project level
Qualifications
- MSc in Statistics or equivalent
- Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research
- Expert knowledge and understanding of the SAS programming
- Expert knowledge and understanding of CDISC ADaM standard
- Expert knowledge and understanding of adaptive designs
- Expert knowledge and understanding of sample size calculation
- Expert knowledge and understanding of relevant regulations and guidelines (e.g. FDA, EMA, ICH)
- Ability to apply advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information
- Ability to consult with clinical investigators, interpret research requirements, and determine statistical analysis strategies
- Strong presentation and communication skills
Additional Information
Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.
Principal Statistician. in Oxford employer: PSI
Contact Detail:
PSI Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Statistician. in Oxford
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. We can help you find opportunities that might not even be advertised yet!
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to statistical analysis in clinical trials. We recommend doing mock interviews with friends or mentors to boost your confidence and refine your answers.
✨Tip Number 3
Showcase your expertise! Bring along examples of your previous work, such as statistical analysis plans or project deliverables, to demonstrate your skills during interviews. We believe this will set you apart from other candidates.
✨Tip Number 4
Don’t forget to apply through our website! It’s the easiest way to get your application noticed, and we’re here to support you throughout the process. Let’s land that Principal Statistician role together!
We think you need these skills to ace Principal Statistician. in Oxford
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in statistical analysis and clinical trials. We want to see how your skills align with the role of Principal Statistician, so don’t be shy about showcasing your expertise in SAS programming and CDISC ADaM standards.
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 background makes you a perfect fit for our team. Remember, we love seeing enthusiasm and a clear understanding of the role!
Showcase Your Communication Skills: As a Principal Statistician, you'll be liaising with various teams. Make sure your application reflects your strong communication skills. Whether it's through your writing style or examples of past collaborations, we want to see that you can effectively convey complex statistical concepts.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our awesome team at StudySmarter!
How to prepare for a job interview at PSI
✨Know Your Stats Inside Out
Make sure you brush up on your statistical principles and methods, especially those relevant to clinical trials. Be ready to discuss your experience with SAS programming and CDISC ADaM standards, as these will likely come up during the interview.
✨Prepare for Scenario Questions
Expect questions that ask how you would handle specific statistical challenges in clinical research. Think of examples from your past work where you successfully led a project or resolved a data issue, and be prepared to explain your thought process.
✨Showcase Your Communication Skills
Since this role involves liaising with various teams and clients, practice articulating complex statistical concepts in simple terms. You might be asked to explain your analysis strategies, so clarity and confidence are key!
✨Familiarise Yourself with Regulations
Brush up on relevant regulations and guidelines like FDA, EMA, and ICH. Being able to discuss how these impact your work will show that you’re not just technically skilled but also aware of the broader context in which you operate.
