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For Companies At a Glance
- Tasks: Lead complex clinical trial projects and provide expert statistical support.
- Company: Dynamic biostatistics consultancy with a focus on innovation.
- Benefits: Competitive salary, professional development, and opportunities for impactful work.
- Why this job: Make a difference in clinical trials and be recognised as a statistical expert.
- Qualifications: PhD or MS in Statistics, SAS programming experience, and strong analytical skills.
- Other info: Collaborative environment with opportunities for mentorship and career growth.
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.
Education
- PhD in Statistics or related discipline, MS in Statistics or related discipline.
Senior Manager, Biostatistician Consultant in London employer: Parexel International
Contact Detail:
Parexel International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Manager, Biostatistician Consultant in London
✨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 advanced techniques. Practice explaining complex concepts in simple terms, as you might need to communicate with non-statisticians too!
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Use our website to find roles that excite you and tailor your approach to each one, highlighting how your skills can make a difference.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. Mention something specific from your conversation to show your genuine interest in the role and the company.
We think you need these skills to ace Senior Manager, Biostatistician Consultant in London
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 relevant projects!
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. We love seeing enthusiasm and a clear understanding of the responsibilities, so make it personal and engaging.
Showcase Your Skills: Highlight your analytical and project management skills in your application. We’re looking for someone who can clearly describe advanced statistical techniques, so don’t forget to mention any relevant software or methodologies you’ve mastered!
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts and submit your materials!
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 showcase your expertise in statistical methods. Brush up on advanced statistical techniques and be ready to discuss how you've applied them in past projects. Prepare examples that highlight your problem-solving skills and your ability to interpret complex data.
✨Understand the Regulatory Landscape
Familiarity with regulatory requirements is crucial for this role. Make sure you can articulate your understanding of ICH guidelines and GCP principles. Be prepared to discuss how these regulations impact statistical processing and analysis in clinical trials, as this will demonstrate your readiness for the position.
✨Showcase Your Project Management Skills
This role requires strong project management abilities. Think of specific instances where you've successfully led projects or managed teams. Highlight your attention to detail and how you've ensured quality control in statistical reports and analysis plans. This will show that you can handle the operational execution aspect of the job.
✨Engage in Business Development Conversations
Since business development is part of the role, prepare to discuss how you've contributed to study design considerations in previous positions. Bring examples of how you've supported budget and proposal development, and be ready to engage in discussions about sample size scenarios during the interview. This will illustrate your ability to contribute to client meetings effectively.
