At a Glance
- Tasks: Lead clinical trial projects and provide statistical oversight for drug development.
- 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 mentor upcoming biostatisticians.
- Why this job: Make a real impact in the healthcare sector while developing your statistical expertise.
- 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 aimee@warmanobrien.com to receive more details surrounding this role and discuss this further!
Data Principal employer: Warman O'Brien
Join a forward-thinking CRO that values innovation and collaboration, offering a dynamic work environment where your expertise as a Data Principal will be recognised and nurtured. With a strong emphasis on employee development, you will have access to mentoring opportunities and the chance to lead impactful projects in the UK and Europe. Enjoy the flexibility of remote work while being part of a supportive team that encourages strategic input and professional growth.
StudySmarter Expert Advice🤫
We think this is how you could land Data Principal
✨Tip Number 1
Network like a pro! Reach out to professionals in the biostatistics field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Show off your skills! Prepare a portfolio showcasing your statistical analyses and projects. This will give potential employers a taste of what you can bring to the table, especially when it comes to clinical trial programmes.
✨Tip Number 3
Practice makes perfect! Get ready for interviews by rehearsing common questions related to statistical methodologies and project management. We recommend doing mock interviews with friends or mentors to boost your confidence.
✨Tip Number 4
Apply through our website! We’ve got loads of opportunities waiting for you. By applying directly, you’ll have a better chance of standing out and getting noticed by hiring managers.
We think you need these skills to ace Data Principal
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that match the job description. Highlight your technical skills and any entrepreneurial flair you've got, as these are key for us at StudySmarter.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for the role. Mention specific projects or experiences that showcase your ability to provide strategic input and leadership.
Showcase Your Statistical Expertise:Since this role involves a lot of statistical oversight, be sure to include examples of your hands-on statistical analysis and methodologies. We want to see how you’ve applied your knowledge in real-world scenarios!
Apply Through Our Website:We encourage you to apply through our website for a smoother process. It helps us keep track of applications and ensures you don’t miss out on any important updates from us at StudySmarter!
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. Since the role requires strong technical skills, you should be able to explain your approach to study design, sample size estimation, and statistical analysis planning clearly.
✨Show Your Leadership Skills
This position involves coaching and mentoring less experienced biostatisticians. Prepare examples of how you've led teams or projects in the past, highlighting your ability to provide technical oversight and strategic input.
✨Familiarise Yourself with Regulatory Requirements
Make sure you understand the relevant regulatory requirements for clinical trials. Be prepared to discuss how you've ensured compliance in previous roles, as this will demonstrate your attention to detail and commitment to quality.
✨Prepare for Technical Questions
Expect to face technical questions during the interview. Practice explaining complex statistical concepts in simple terms, as you may need to communicate these ideas to non-statistical personnel or stakeholders.
