Principal Biostatistician

Veristat; France; À distance; EUR 60 000 - 90 000; Plein temps

Résumé du poste

A global clinical research organization in France is seeking a Principal Biostatistician to provide statistical input in clinical trial development. This role requires expertise in analyzing clinical data and the ability to function as a lead statistician. Candidates should have a PhD with 5 years of experience or a Master’s degree with 8 years in the field, along with familiarity in SAS or SPSS. The company offers a flexible and inclusive work culture with remote work options.

Prestations

Flexible time off

Paid holidays

Medical insurance

Tuition reimbursement

Retirement plans

Remote working

Qualifications

• 5+ years of biostatistical experience in clinical trials or health research environment.
• 8+ years of biostatistical experience with Master's degree.
• Familiarity with moderately complex statistical methods applicable to Phase I-IV clinical trials.

Responsabilités

• Provide statistical input into Phase I - IV clinical trial development.
• Perform analysis of clinical trial data.
• Function as a lead statistician on clinical trials.

Connaissances

Excellent written and oral communication skills

Detail orientation

Ability to work under tight timelines

Formation

PhD in Statistics or Biostatistics or related field

Master’s degree in Statistics or Biostatistics or related field

Outils

SAS

SPSS

Microsoft Word

Microsoft Excel

Description du poste

Overview

Principal Biostatistician

The Principal Biostatistician provides statistical input into Phase I - IV clinical trial development, performs the analysis of clinical trial data, and provides statistical input into the reporting of clinical trial results. The Principal Biostatistician can work independently and function as a lead statistician on clinical trials.

Why Veristat

Make an Impact at Veristat!

Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.

• 105+ approved therapies for marketing applications prepared by Veristat
• 480+ oncology projects in the past 5 years
• 350+ rare disease projects delivered in the past 5 years
• Flexible, inclusive culture — 70% remote workforce, 66% women-led teams
• Learn more about our core values here!

What we offer

Benefits vary by location and may include :

• Remote working
• Flexible time off
• Paid holidays
• Medical insurance
• Tuition reimbursement
• Retirement plans

What we look for

• PhD degree in Statistics, Biostatistics, or related field, and 5 years of biostatistical experience in the clinical trials or health research environment OR a Master’s degree in Statistics, Biostatistics, or related field, and 8 years of biostatistical experience in the clinical trials or health research environment.
• Excellent written and oral communication skills including grammatical / technical writing skills and familiarity with moderately complex statistical methods that apply to Phase IIV clinical trials are required.
• Familiarity with SAS, SPSS or other statistical software package.
• Proficiency in Microsoft Word and Excel.
• Strong level of detail orientation.
• Ability to work on multiple tasks under tight timelines.

Automated Decision Making : All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.

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Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.