At a Glance
- Tasks: Lead clinical trial projects, providing statistical oversight and mentoring junior biostatisticians.
- Company: Modern CRO with a focus on innovation and collaboration.
- Benefits: Flexible remote work, competitive salary, and opportunities for professional growth.
- Other info: Join a dynamic team and contribute to meaningful clinical research.
- Why this job: Make a real impact in drug development while working with cutting-edge statistical methodologies.
- Qualifications: Ph.D. or Master's in statistical science or related fields required.
The predicted salary is between 60000 - 80000 € per year.
We have recently partnered with this modern thinking, CRO, who are looking for biostatisticians to join their team, to expand their outreach in the UK / Europe. You will need strong technical skills and also an entrepreneurial flair and the ability to offer strategic input.
Key Accountabilities:
- Work with a leader of the Statistical Operations management team to manage clinical trial programs/projects from one or multiple clients.
- Provide day to day technical and operational leadership to project teams supporting these programs/projects.
- Provide statistical oversight on projects in the assigned drug development programs/projects, ensuring sound statistical methodologies in study design, sample size estimation, statistical analysis planning, statistical modeling, data handling, analysis, and reporting.
- Coach, mentor, develop, and provide technical review, advice and expertise to less experienced Biostatisticians as well as Statistical Programmers assigned to the program/projects.
- Provide statistical input in protocol design and development.
- Participate in the writing of trial protocols and research proposals.
- Write Statistical Analysis Plans, Statistical Reports, and statistical methodologies sections of Clinical Study Reports.
- Perform peer review of SAPs and other technical documents written by others.
- Perform hands on statistical analysis and modeling, and maintain expertise in state-of-the-art statistical methodology and regulatory requirements.
- Review and confirm ADaM dataset specifications.
- Perform quality control activities on ADaM datasets programmed by other statistical programmers and biostatisticians.
- Provide statistical consultation to medical and clinical trial personnel for the publication of trial results, and participate in the writing of abstracts, manuscripts, posters, and presentations.
- Ensure all study level as well as drug program level statistical and programming activities are conducted in compliance with relevant regulatory requirements.
- Interact with regulatory agencies and support sponsor in new drug application.
Qualifications and Experience:
- A Ph.D. degree in statistical science, mathematical analysis or related fields
- OR A Master’s degree in the above fields
Interested? Drop me a message or send your CV to receive more details surrounding this role and discuss this further!
Principal Biostatistician in Bath employer: Warman O'Brien
Join a forward-thinking CRO that values innovation and collaboration, offering a dynamic work environment for Principal Biostatisticians. With a strong emphasis on employee development, you will have the opportunity to mentor junior staff while engaging in meaningful projects that impact drug development across the UK and Europe. Enjoy the flexibility of remote work combined with a supportive culture that encourages strategic input and professional growth.
StudySmarter Expert Advice🤫
We think this is how you could land Principal Biostatistician in Bath
✨Tip Number 1
Network like a pro! Reach out to your connections in the biostatistics field, attend industry events, and join relevant online forums. The more people you know, the better your chances of landing that Principal Biostatistician role.
✨Tip Number 2
Show off your skills! Prepare a portfolio showcasing your statistical analysis projects and methodologies. When you get the chance to chat with potential employers, share your insights and experiences to demonstrate your expertise.
✨Tip Number 3
Be proactive! Don’t just wait for job postings; reach out directly to companies you admire. Express your interest in their work and how you can contribute as a Principal Biostatistician. You never know what opportunities might arise!
✨Tip Number 4
Apply through our website! We’ve got a range of exciting roles waiting for talented biostatisticians like you. By applying directly, you’ll have a better chance of getting noticed and landing that dream job.
We think you need these skills to ace Principal Biostatistician in Bath
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that match the Principal Biostatistician role. Highlight your technical expertise and any entrepreneurial projects you've led, as these are key for us.
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 you can contribute to our team. Be sure to mention any relevant projects or experiences that showcase your strategic input.
Showcase Your Technical Skills:Since this role requires strong technical skills, don’t shy away from detailing your experience with statistical methodologies, data analysis, and programming. We want to see your hands-on experience and how you’ve applied it in real-world scenarios.
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 modern-thinking team!
How to prepare for a job interview at Warman O'Brien
✨Know Your Stats
Brush up on your statistical methodologies and be ready to discuss them in detail. This role requires a strong technical background, so be prepared to explain your experience with study design, sample size estimation, and statistical analysis planning.
✨Show Your Leadership Skills
Since you'll be providing day-to-day leadership to project teams, think of examples where you've successfully led a team or mentored others. Be ready to share how you can coach less experienced biostatisticians and contribute to their development.
✨Prepare for Technical Questions
Expect questions that dive deep into your technical expertise. Review common statistical models and methodologies relevant to clinical trials, and be prepared to discuss how you've applied these in past projects.
✨Understand Regulatory Requirements
Familiarise yourself with the regulatory landscape surrounding drug development. Be ready to discuss how you've interacted with regulatory agencies in the past and how you ensure compliance in your work.
