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For Companies At a Glance
- Tasks: Lead complex clinical trial projects and provide expert statistical support.
- Company: Join a leading biostatistics consultancy with a focus on innovation.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Why this job: Make a significant impact in clinical trials and enhance your statistical expertise.
- Qualifications: PhD or MS in Statistics, SAS programming experience, and strong analytical skills.
- Other info: Collaborative environment with opportunities to mentor and lead.
The predicted salary is between 54000 - 84000 £ per year.
The Principal Biostatistician works independently on all level complexity clinical trial projects, often with major regulatory impact. The person will be recognized internally and externally as a statistical expert.
Key Accountabilities
- Operational Execution: Provide broad statistical support, including trial design, protocol and CRF development on specific studies. Lead production and quality control of randomization, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents. Perform sample-size calculations, generate randomization lists and write statistical methodology sections for inclusion in study protocols. Provide statistical input into Data Monitoring Committee (DMC) activities, including development of DMC charters and analysis plans. Provide a supporting role as a non-voting independent statistician providing data and analysis for DMC review.
- Business Development: Support of Business Development, by actively contributing to study design considerations in internal and client meetings, providing and discussing sample size scenarios, support of budget and proposal development, attending and preparing bid defense meetings.
- General Activities: Understand regulatory requirements related to the specific therapeutic areas and the implications for statistical processing and analysis. Understand, apply and provide training in extremely advanced and sometimes novel statistical methods. Contribute to the development and delivery of internal and external statistical training seminars and courses. Review position papers based on current good statistical practice. Interact with clients and regulatory authorities. Review publications and clinical study reports. Travel to, attend, and actively contribute to all kinds of client meetings as appropriate (e.g. discussing analysis concepts, presenting and discussing study results). Additional responsibilities as defined by supervisor/manager.
Skills:
- Good analytical skills.
- Good project management skills.
- Professional attitude.
- Attention to detail.
- Thorough understanding of statistical issues in clinical trials.
- Ability to clearly describe advanced statistical techniques and interpret results.
- Familiarity with regulatory/research guidelines on drug development, GCP, and statistical principles (especially ICH guidelines).
- Prior experience with SAS programming required.
- Ability to work independently.
- Good mentoring/leadership skills.
- Good business awareness/business development.
Knowledge and Experience: The knowledge of pharmacokinetic data is an advantage. Competent in written and oral English.
Education: PhD in Statistics or related discipline, MS in Statistics or related discipline.
Senior Manager, Biostatistician Consultant employer: Parexel International
Contact Detail:
Parexel International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Manager, Biostatistician Consultant
✨Tip Number 1
Network like a pro! Reach out to your connections in the biostatistics field and let them know you're on the lookout for opportunities. Attend industry events or webinars to meet potential employers and showcase your expertise.
✨Tip Number 2
Prepare for interviews by brushing up on your statistical knowledge and being ready to discuss complex trial designs. We recommend practising common interview questions and even doing mock interviews with friends or colleagues.
✨Tip Number 3
Showcase your skills through a portfolio! If you have previous projects or reports, compile them into a portfolio that highlights your analytical skills and project management experience. This can really set you apart from other candidates.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities waiting for talented individuals like you. Keep an eye on our job listings and make sure your application stands out by tailoring it to each role.
We think you need these skills to ace Senior Manager, Biostatistician Consultant
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your experience in biostatistics and clinical trials. We want to see how your skills align with the key accountabilities mentioned in the job description, so don’t hold back on showcasing your expertise!
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 Senior Manager, Biostatistician Consultant role. Be sure to mention specific projects or experiences that demonstrate your statistical prowess and leadership skills.
Showcase Your Analytical Skills: Since this role requires good analytical skills, make sure to include examples of how you've applied these in past projects. Whether it's through sample-size calculations or leading statistical reports, we want to see your thought process and results!
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 at StudySmarter!
How to prepare for a job interview at Parexel International
✨Know Your Stats Inside Out
As a Senior Manager, Biostatistician Consultant, you'll need to demonstrate your expertise in statistical methods. Brush up on advanced statistical techniques and be ready to discuss how you've applied them in clinical trials. Prepare examples that showcase your analytical skills and attention to detail.
✨Familiarise Yourself with Regulatory Guidelines
Understanding regulatory requirements is crucial for this role. Make sure you’re well-versed in ICH guidelines and GCP principles. During the interview, be prepared to discuss how these regulations impact statistical processing and analysis in clinical trials.
✨Showcase Your Project Management Skills
This position requires strong project management abilities. Think of specific instances where you've successfully led projects or contributed to study design considerations. Highlight your experience in managing timelines, budgets, and team dynamics to show you can handle complex trial projects.
✨Engage in Business Development Conversations
Since business development is part of the role, be ready to discuss how you can contribute to client meetings and proposal development. Prepare to share your thoughts on sample size scenarios and how you can support budget discussions. This will show your understanding of the business side of biostatistics.
