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Principal Statistician Consultant-R&I (Respiratory & Immunology) REMOTE@EU/UK

1 month ago
Europe, United Kingdom
Contract
Lead
Data Scientist
Data Science and Analytics
R Statistics
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ClinChoice

ClinChoice

ClinChoice is a leading full-service contract research organization (CRO) that provides high-quality solutions to clients in the pharmaceutical, biotechnology, medical device, and consumer products sectors, focusing on accelerating the development and ...

Professional Services
1K-5K
Founded 1995
View All Jobs 3

Description

  • Lead protocol development, including study design, sample size calculation, randomization, and statistical analysis plans for assigned studies.
  • Provide statistical oversight to studies and ensure quality and consistency with project requirements.
  • Ensure data for statistical analyses are complete, accurate, and consistent.
  • Prepare statistical analysis plans and ensure timely, accurate statistical input into reports and decisions.
  • Evaluate the validity of analyses and propose alternative analysis strategies when needed.
  • Review and correct statistical tables, figures, data listings, and report text for accuracy and consistency.
  • Write and review the statistical methods sections of reports and ensure adherence to report guidelines.
  • Mentor peers on statistical methodology and train less experienced statisticians.
  • Coordinate and manage statistician assignments across projects to support on-time, high-quality delivery.
  • Interpret study data for internal clinical and statistical teams and communicate findings to client counterparts.

Requirements

  • MS or PhD in Statistics, Biostatistics, or a related field.
  • PhD with 2-4 years of experience or MS with 5-7 years of experience.
  • Strong SAS skills.
  • Experience programming in both SAS and R.
  • Lead experience with CRO oversight.
  • Experience in Respiratory & Immunology, preferably asthma studies.
  • Strong oral and written communication skills with the ability to communicate internally and with clients.
  • Understanding of statistics, the drug development process, and relevant FDA regulations.
  • Pharmaceutical, CRO, or related industry experience with clinical trials and interaction with regulatory agencies, especially the FDA.
  • Experience working on study readouts, including tables, listings, and figures.

Benefits

  • Opportunity to work directly with a single sponsor while employed through a global CRO.
  • Remote work designation indicated by #LI-Remote.
  • Supportive culture with a focus on professional development and close management/training.
  • Work for a global full-service CRO with a broad international presence.
  • Equal opportunity employer committed to diversity and inclusion.

Interested in this position?

Apply directly on the company website

Apply Now

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