Director Biostatistician

Director Biostatistician

Woking Full-Time 48000 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead statistical analyses and provide expertise for clinical development projects.
  • Company: Join a forward-thinking company dedicated to advancing healthcare through innovative research.
  • Benefits: Enjoy flexible working options, professional development opportunities, and a collaborative culture.
  • Why this job: Make a real impact in healthcare while working with cutting-edge data and methodologies.
  • Qualifications: Advanced degree in statistics or related field; experience in clinical trials preferred.
  • Other info: Opportunity to attend conferences and enhance your statistical expertise.

The predicted salary is between 48000 - 72000 £ per year.

Job responsibilities (but not limited to):

  • Coordinates, provides, and delivers methodological and statistical expertise and/or statistical analyses.
  • Supports both the Clinical Development portfolio as well as Strategic Medical Affairs in their support to Affiliates, thereby complying with international, regulatory guidelines and policies and standards.
  • Directs the operational aspects of statistical work as outsourced to CROs.
  • Manages several projects and works in more than one therapeutic area.
  • Attends and presents at external meetings for Statistics (such as Investigators Meetings, Regulatory Agencies, Advisory Boards).
  • Provides adequate and qualified statistical and methodological support to EPD, e.g. input into Clinical Development Plans, and study protocols.
  • Responsible for appropriate statistical methodology and endpoint definitions as part of the design of clinical studies and for the associated sample size determination.
  • Writes and/or reviews the statistical part of the protocol.
  • Responsible for briefing the CRO to ensure appropriate conduct of statistical analysis of EPD Clinical Development studies, which entails review of the statistical analysis plan, participation in Blind Data Reviews, and review of study report tables, listings, and figures.
  • Approves the lock of the database and requests unblinding of the study for subsequent analysis.
  • Together with the Clinician, clarifies and communicates the results and conclusions to ensure the correct interpretation of the results by different users.
  • Supports dossier submissions and answers statistical questions related to the file.
  • For the purpose of integrated analyses of internal compound databases that are accumulating, writes the strategic and more detailed integration plans in cooperation with Clinical and ensures proper execution.
  • Fully exploits the potential of the data to enhance the knowledge of the compound through data integration and data utilization activities (meta-analyses, data explorations).
  • Manages external study statisticians working on the analysis of EPD clinical trial data.
  • Briefs CROs on methodological and statistical deliverables.
  • Reviews statistical literature and attends conferences and courses to ensure high statistical expertise and maintain proficiency.
  • Works with other statisticians to acquire knowledge on new/improved statistical methodology.
  • Keeps up to date in relevant statistical expertise and clinical content expertise.

Director Biostatistician employer: Tech Observer

As a Director Biostatistician at our company, you will thrive in a dynamic and collaborative work environment that prioritises innovation and professional growth. We offer competitive benefits, including ongoing training opportunities and a supportive culture that values your contributions to impactful clinical research. Located in a vibrant area, our team enjoys a healthy work-life balance while making significant strides in advancing medical science.
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Contact Detail:

Tech Observer Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Director Biostatistician

✨Tip Number 1

Network with professionals in the biostatistics field, especially those who have experience in clinical development. Attend relevant conferences and workshops to meet potential colleagues and learn about the latest trends and methodologies.

✨Tip Number 2

Familiarise yourself with the specific regulatory guidelines and standards that govern clinical trials. This knowledge will not only enhance your expertise but also demonstrate your commitment to compliance during interviews.

✨Tip Number 3

Prepare to discuss your experience with managing multiple projects across different therapeutic areas. Highlight any successful collaborations with CROs and how you ensured the quality of statistical analyses.

✨Tip Number 4

Stay updated on the latest statistical methodologies and tools. Being able to discuss recent advancements or techniques during your interview can set you apart as a knowledgeable candidate who is eager to contribute to our team.

We think you need these skills to ace Director Biostatistician

Advanced Statistical Analysis
Clinical Trial Design
Regulatory Compliance Knowledge
Project Management
Statistical Software Proficiency (e.g., SAS, R)
Data Integration Techniques
Meta-Analysis Skills
Communication and Presentation Skills
Collaboration with CROs
Sample Size Determination
Statistical Methodology Development
Attention to Detail
Problem-Solving Skills
Knowledge of Therapeutic Areas

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in biostatistics, clinical development, and project management. Emphasise any previous roles where you coordinated statistical analyses or worked with CROs.

Craft a Strong Cover Letter: In your cover letter, clearly articulate your understanding of the role's responsibilities. Mention specific experiences that demonstrate your ability to manage multiple projects and provide statistical expertise in clinical settings.

Showcase Your Methodological Knowledge: Include examples of statistical methodologies you have employed in past projects. Discuss your experience with endpoint definitions, sample size determination, and any contributions to clinical study protocols.

Highlight Communication Skills: Since the role involves presenting at external meetings and collaborating with various stakeholders, emphasise your communication skills. Provide examples of how you've effectively communicated complex statistical concepts to non-statistical audiences.

How to prepare for a job interview at Tech Observer

✨Showcase Your Statistical Expertise

Make sure to highlight your experience with statistical methodologies and analyses during the interview. Be prepared to discuss specific projects where you applied these skills, especially in clinical development and regulatory contexts.

✨Demonstrate Project Management Skills

Since the role involves managing multiple projects across various therapeutic areas, be ready to share examples of how you've successfully coordinated projects in the past. Discuss your approach to prioritising tasks and managing timelines.

✨Prepare for Technical Questions

Expect technical questions related to statistical analysis plans, sample size determination, and endpoint definitions. Brush up on these topics and be ready to explain your thought process and decision-making in previous roles.

✨Communicate Clearly and Effectively

As the role requires collaboration with clinicians and external stakeholders, practice articulating complex statistical concepts in a clear and concise manner. This will demonstrate your ability to communicate effectively with non-statistical audiences.

Director Biostatistician
Tech Observer
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  • Director Biostatistician

    Woking
    Full-Time
    48000 - 72000 £ / year (est.)

    Application deadline: 2027-06-20

  • T

    Tech Observer

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