Activez les alertes d’offres d’emploi par e-mail !

Principal Statistician

Warman O'Brien

Nice

À distance

EUR 60 000 - 90 000

Plein temps

Il y a 4 jours
Soyez parmi les premiers à postuler

Générez un CV personnalisé en quelques minutes

Décrochez un entretien et gagnez plus. En savoir plus

Repartez de zéro ou importez un CV existant

Résumé du poste

A leading global biometric CRO is seeking experienced Principal Statisticians to join their FSP team. Successful candidates will work on significant clinical trials in cardio, renal, and metabolic fields while enjoying a recognized outstanding workplace with structured training and flexible hours.

Prestations

Competitive salary and benefits package
Structured training and development plans
Condensed hours for shorter workweek

Qualifications

  • Experience within the pharmaceutical industry.
  • Good awareness of clinical trial issues, design, and implementation.
  • Familiarity with GCP and regulatory requirements.
  • Experience of writing SAPs and protocols.

Responsabilités

  • Work as a statistician on cardio, renal & metabolic clinical trials.
  • Produce and validate complex outputs to excellent quality.
  • Adhere to deliverable timelines.

Connaissances

Biostatistics
Statistics
Data Management
Clinical Trial Design

Formation

PhD or MSc in Biostatistics, Statistics or a related discipline

Description du poste

Award-winning global biometric CRO have multiple opportunities for experienced Principal Statisticians to join its growing FSP team.

Partnering with top pharma, biotech, and medical device companies, they deliver high-quality biostatistics, programming, data management, and data science services.

What you will be doing :

The successful candidates will be working as a statistician on cardio, renal & metabolic clinical trials; producing and validating complex outputs to excellent quality whilst adhering to deliverable timelines.

What you will need :

  • Educated to PhD or MSc in Biostatistics, statistics or a related discipline
  • Experience within the pharmaceutical industry to have a good awareness of clinical trial issues, design, and implementation.
  • Familiarity with GCP and regulatory requirements
  • Experience of writing SAPs, protocols

What’s in it for you :

  • Recognized as an outstanding workplace, committed to employee engagement, satisfaction, and work-life balance.
  • Structured training, development plans, and a supportive, friendly environment.
  • Condensed hours for a shorter workweek.
  • Competitive salary and benefits package.
  • Fully remote role available in France.

What to do next :

If this opportunity is of interest, please apply now with your CV as the organisation are looking to welcome Principal Statisticians onboard as soon as possible.

Not what you’re looking for?

Please contact Mark O'Brien at [emailprotected] for a confidential discussion about potential other opportunities in France and across Europe.

Obtenez votre examen gratuit et confidentiel de votre CV.
ou faites glisser et déposez un fichier PDF, DOC, DOCX, ODT ou PAGES jusqu’à 5 Mo.