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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: Dynamic role with opportunities to mentor and lead within a collaborative environment.
The predicted salary is between 72000 - 108000 £ 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.
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 in Uxbridge employer: Parexel
Contact Detail:
Parexel Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Manager, Biostatistician Consultant in Uxbridge
✨Network Like a Pro
Get out there and connect with people in the industry! Attend conferences, webinars, or local meetups related to biostatistics. You never know who might have a lead on your dream job or can introduce you to someone influential.
✨Show Off Your Expertise
When you get the chance to chat with potential employers, don’t hold back! Share your knowledge about advanced statistical methods and how they apply to clinical trials. This will help you stand out as a true expert in your field.
✨Ace the Informal Interview
If you land an informal chat or coffee meeting, treat it like a mini-interview. Prepare some questions about their projects and share your insights on trial design and statistical analysis. This shows you're genuinely interested and knowledgeable.
✨Apply Through Our Website
Don’t forget to check out our website for job openings! Applying directly through us not only makes your application more visible but also shows your enthusiasm for joining our team at StudySmarter.
We think you need these skills to ace Senior Manager, Biostatistician Consultant in Uxbridge
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Senior Manager, Biostatistician Consultant role. Highlight your expertise in statistical methods and any relevant project management experience to catch our eye!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this position. Mention specific projects you've worked on that relate to clinical trials and how you can contribute to our team.
Showcase Your Analytical Skills: We love seeing strong analytical skills in action! In your application, provide examples of how you've tackled complex statistical problems or contributed to successful trial designs. This will demonstrate your expertise and problem-solving abilities.
Apply Through Our Website: Don't forget to apply 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 the StudySmarter family!
How to prepare for a job interview at Parexel
✨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 understand ICH guidelines and GCP principles. During the interview, demonstrate your knowledge of how these regulations impact statistical processing and analysis in clinical trials.
✨Showcase Your Project Management Skills
This position requires strong project management abilities. Be prepared to discuss how you've successfully led projects in the past, including your approach to quality control and collaboration with cross-functional teams. Highlight any experience you have with trial design and protocol development.
✨Engage in Business Development Conversations
Since business development is part of the role, think about how you can contribute to study design considerations. Prepare to discuss sample size scenarios and your experience in client meetings. Show that you can not only crunch numbers but also communicate effectively with clients and stakeholders.
