At a Glance
- Tasks: Lead statistical activities for global clinical trials and collaborate with international teams.
- Company: Join a leading biostatistics team in a dynamic clinical research environment.
- Benefits: Competitive salary, professional development, and opportunities for global collaboration.
- Other info: Exciting career growth opportunities in a supportive and innovative workplace.
- Why this job: Make a real impact on clinical research and enhance your statistical expertise.
- Qualifications: MSc in Statistics and expert knowledge in SAS programming and clinical research standards.
The predicted salary is between 60000 - 80000 € per year.
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.
In this role, you will:
- 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
Principal Statistician in Oxford employer: Psi CRO Ag
As a Principal Statistician at our company, you will be part of a dynamic and collaborative work culture that values innovation and excellence in clinical research. We offer competitive benefits, including professional development opportunities and a supportive environment that encourages growth and learning. Located in a vibrant area, our team enjoys a balance of work and life, making it an ideal place for those seeking meaningful and rewarding employment in the field of biostatistics.
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 all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for interviews by brushing up on your statistical knowledge and being ready to discuss your experience with clinical trials. We recommend practising common interview questions and even doing mock interviews with friends or mentors.
✨Tip Number 3
Showcase your skills! Create a portfolio of your work, including any statistical analyses or projects you've led. This will give potential employers a tangible sense of what you can bring to the table.
✨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 about their job search!
We think you need these skills to ace Principal Statistician in Oxford
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Principal Statistician role. Highlight your experience with clinical trials, statistical analysis, and any relevant software like SAS. 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 expertise aligns with our needs. Don’t forget to mention any experience with CDISC ADaM standards or adaptive designs.
Showcase Your Communication Skills:Since this role involves liaising with various teams, make sure to highlight your communication skills in your application. We love candidates who can clearly convey complex statistical concepts to different audiences!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Psi CRO Ag
✨Know Your Stats Inside Out
Make sure you brush up on your statistical principles and methods, especially those relevant to clinical trials. Be prepared to discuss your experience with SAS programming and CDISC ADaM standards, as these will likely come up during the interview.
✨Showcase Your Communication Skills
Since this role involves liaising with various teams and stakeholders, practice articulating complex statistical concepts in a clear and concise manner. Think of examples where you've successfully communicated statistical findings or led training sessions.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Prepare to discuss how you would handle statistical issues during clinical trials or how you would approach developing a statistical analysis plan.
✨Familiarise Yourself with Regulations
Brush up on relevant regulations and guidelines like FDA, EMA, and ICH. Being able to demonstrate your understanding of these will show that you're not just technically skilled but also aware of the compliance landscape in clinical research.
