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Principal Biostatistician - Remote
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Principal Biostatist....
drjobs Principal Biostatistician - Remote العربية

Principal Biostatistician - Remote

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1 Vacancy
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Job Location

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London - UK

Monthly Salary

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Not Disclosed

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Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 2715674

Our Senior Biostatisticians perform adhoc or exploratory analyses to support submission or Health Authority Questions. Having exposure to regulatory work experience is a bonus for example if you understand the regulatory questions and translating them to statistical problems collaborating effectively with clinical and regulatory colleagues. Supporting medium complexity clinical trials (starting from Design to Archival experience) and supporting some projectlevel activities.
As a Principal Biostatistician your responsibilities will include:

  • Providing statistical support to clinical studies
  • Participating in the development of study protocols including participation in study design discussions and sample size calculations
  • Reviewing CRFs and data review guidelines; developing statistical analysis plans (SAPs) including analysis dataset and TLG specifications
  • Performing statistical analyses and interpreting statistical results
  • Preparing clinical study reports including integrated summaries for submissions
  • Utilizing your strong communication skills to present and explain the methodology and consequences of decisions.


To be successful in this position you will have:

  • Masters degree in statistics or a related discipline. Ph.D. strongly desired.
  • 8 years supporting clinical trials in the Pharmaceutical or Biotechnology industry.
  • Experience working for a CRO is strongly desired.
  • Experience in sample size calculation protocol concept development protocol development SAP and preparing clinical study reports including integrated summaries for submissions.
  • Good SAS programming skills for QCing critical outputs Efficacy/Safety tables and working closely with Programmers. Knowledge of R programming is a plus.
  • Solid understanding implementation of CDISC requirements for regulatory submissions.
  • Adept in ADaM specifications generation and QC of datasets
  • The ability to build strong external internal relationships and motivate a regional or global team.
  • Very effective communicator: able to explain methodology and consequences of decisions in lay terms.

Please use the below link for job application and quicker response.

Remote Work :

No

Employment Type

Full Time

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