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Manager, Biostatistics

TN United Kingdom

United Kingdom

On-site

GBP 60,000 - 100,000

Full time

2 days ago
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Job summary

An established industry player is seeking a Manager of Biostatistics to join their dynamic team. This role offers a unique opportunity to leverage your statistical expertise in the development of transformative gene therapies for patients with rare diseases. As the lead statistician, you will play a crucial role in clinical studies, ensuring data quality and regulatory compliance. This position is perfect for a self-starter with strong project management skills who can communicate complex statistical concepts effectively. Join a forward-thinking company where your contributions can make a significant impact on patients' lives.

Qualifications

  • Solid experience as a Statistician in drug development.
  • Proficiency with SAS and knowledge of CDISC standards.

Responsibilities

  • Lead statistician for multiple studies, providing statistical input.
  • Review and write Statistical Analysis Plans and oversee vendors.

Skills

Statistical methodologies
SAS
R
CDISC standards
Bayesian methodology
Time management
Project management
Interpersonal skills

Education

MSc in Statistics
PhD in Statistics

Tools

SAS
R

Job description

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Reporting to: Executive Director, Biostatistics

Job Summary

The Manager, Biostatistics at Orchard Therapeutics is a key member of a cross-functional team working to provide transformative gene therapies to patients with rare diseases. Reporting to the Executive Director, Biostatistics, this role provides a unique opportunity to contribute your statistical expertise to all aspects of clinical drug development in a dynamic environment.

Responsibilities

In this role you will be expected to take on the responsibilities of the lead statistician for a number of studies. As a key member of the Clinical Program Team, you will be required to provide input to all statistical aspects of clinical studies and submissions paying particular regard to data and statistical quality, relevance to regulatory requirements, and scientific validity.

Key responsibilities will include:

· Statistical input into protocol development including advice on study design, sample size calculations, and writing the statistical section of the protocol

· Review of Case Report Forms and all data management documents

· Writing and/or reviewing Statistical Analysis Plans including design of table shells

· Oversight of vendors providing statistical services, including updates to Trial Master Files as required

· Programming of TFLs to support CSRs, ad-hoc requests and regular regulatory safety updates

· Statistical input into CSRs and submission documents including preparation of statistical methods and input into results sections incorporating statistical conclusions

· Response to questions from regulatory authorities.

Requirements

Experience and Knowledge

· Solid experience working as a Statistician in drug development

· Experience in applying a range of statistical methodologies to clinical trial and real-world data

· Proficiency with SAS required, experience with R an advantage

· Good knowledge of CDISC standards

· Experience with Bayesian methodology would be an advantage

· Experience working in rare diseases or in trials in small populations would be an advantage.

· Proven track record of providing on-time, high quality deliverables (including SAPs/shells, ad hoc TFLs, input into CSRs and regulatory documents)

· Good time management: ability to prioritize and adapt to rapidly changing requirements

· Self-starter with the ability to work on a cross-functional team

· Demonstrable project management and interpersonal skills

· Ability to communicate complex statistical concepts to non-statisticians

Education

· MSc or PhD in statistics or related discipline

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