At a Glance
- Tasks: Lead clinical trial projects and provide statistical expertise to teams.
- 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 shape the future of clinical trials.
- Why this job: Make a real impact in drug development while mentoring the next generation of biostatisticians.
- 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 Worcester 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 Worcester
✨Tip Number 1
Network like a pro! Reach out to your connections in the biostatistics field, attend industry events, and engage on platforms like LinkedIn. We can’t stress enough how personal connections can lead to job opportunities.
✨Tip Number 2
Prepare for interviews by brushing up on your technical skills and being ready to discuss your past projects. We recommend practising common interview questions and having examples ready that showcase your strategic input and leadership abilities.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. We suggest checking out our website for tailored job listings that match your expertise in biostatistics.
✨Tip Number 4
Follow up after interviews! A simple thank you email can go a long way in keeping you top of mind. We believe showing genuine interest can set you apart from other candidates.
We think you need these skills to ace Principal Biostatistician in Worcester
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Principal Biostatistician role. Highlight your technical skills and any entrepreneurial experiences that align with the job description. We want to see how you can bring value to our team!
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 experience fits with our modern thinking approach. Let us know what makes you the perfect fit for this role.
Showcase Your Leadership Skills:Since this role involves coaching and mentoring, be sure to highlight any leadership experiences you've had. We love seeing examples of how you've guided others in your previous roles, so don’t hold back!
Apply Through Our Website:We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you get all the updates directly from us. We can't wait to hear from you!
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 foundation, so make sure you can explain concepts like sample size estimation and statistical modelling clearly.
✨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 prepared to share how you approach coaching less experienced biostatisticians.
✨Familiarise Yourself with Regulatory Requirements
Understand the regulatory landscape relevant to clinical trials. Be ready to discuss how you ensure compliance in your work, especially when it comes to statistical analysis plans and reporting.
✨Prepare for Scenario Questions
Expect questions that ask how you would handle specific challenges in clinical trial projects. Think about past experiences where you had to provide strategic input or solve complex problems, and be ready to articulate your thought process.
