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- Tasks: Lead statistical activities for global clinical trials and collaborate with international teams.
- Company: Dynamic global company dedicated to improving lives through medical science.
- Benefits: Competitive salary, supportive work culture, and opportunities for professional growth.
- Other info: Join a team that values your input and offers a straightforward recruitment process.
- Why this job: Make a real impact in clinical research and contribute to life-changing medicines.
- Qualifications: MSc in Statistics and expert knowledge in clinical research and SAS programming.
The predicted salary is between 60000 - 80000 £ per year.
We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
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
- 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
- Full working proficiency in English
- 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 pharmacokinetics principles, concepts, methods and standards used in clinical research, including the conduct NCL and population PK analysis
- Expert knowledge and understanding of Phoenix WinNonlin and NLME
- Expert knowledge and understanding of relevant regulations and guidelines (e.g. FDA, EMA, ICH)
- Ability to apply a range of 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
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 (Pharmacokinetics) in Oxford employer: PSI CRO
Contact Detail:
PSI CRO Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Statistician (Pharmacokinetics) 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 that can land you that dream job.
✨Tip Number 2
Prepare for interviews by researching the company and understanding their values. We want to see how you fit into our culture, so be ready to share how your skills align with our mission of changing lives through medical science.
✨Tip Number 3
Showcase your expertise! Bring examples of your previous work, especially any statistical analyses or projects related to pharmacokinetics. We love seeing how you’ve applied your knowledge in real-world scenarios.
✨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’re here to support you throughout the recruitment process, making it as smooth as possible.
We think you need these skills to ace Principal Statistician (Pharmacokinetics) 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 statistical analysis in clinical trials and any relevant software skills, like SAS or Phoenix WinNonlin. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about pharmacokinetics and how your expertise can contribute to our mission. Keep it engaging and personal – we love to see your personality come through!
Showcase Your Skills: In your application, don’t just list your qualifications; demonstrate them! Include specific examples of projects where you applied advanced statistical techniques or led teams. This helps us understand your practical experience and how you can fit into our dynamic team.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It’s straightforward, and you’ll get to see all the details about the role and our company culture. Plus, it helps us keep track of your application better!
How to prepare for a job interview at PSI CRO
✨Know Your Stats
Brush up on your statistical principles and methods, especially those relevant to pharmacokinetics. Be ready to discuss how you've applied these in past projects, as this will show your expertise and confidence in the field.
✨Familiarise with CDISC ADaM Standards
Make sure you understand the CDISC ADaM standards inside out. Prepare examples of how you've developed or reviewed study protocols and statistical analysis plans, as this will demonstrate your practical experience and attention to detail.
✨Communication is Key
Since you'll be acting as a communication line for various teams, practice articulating complex statistical concepts in simple terms. Think of scenarios where you've successfully communicated with non-statistical stakeholders and be ready to share those experiences.
✨Prepare for Audits
Get familiar with the audit process related to statistics. Be prepared to discuss your role in past audits and how you ensured compliance with regulations. This shows that you understand the importance of quality systems in clinical research.