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Junior Statistician / Statistical Programmer in Immuno-Oncology

Fonction : Clinical Development

Début de mission : 07-06-2019

Publiée le : 07-06-2019

Type de contrat : CDI

Présentation du poste

Job Posting at Innate Pharma: Junior Statistician / Statistical Programmer in Immuno-Oncology

In the Clinical Development Department, you will be a core team member within a matrix organization. You will be actively involved in the development of Innate Pharma's (IPH) immuno-oncology (IO) products through approval.

Within the biometrics unit, your main mission will focus on providing support to statistical programming, data analysis, clinical trial design, and ensuring the quality control (QC) of statistical and data management programs.

Main responsibilities and key tasks:

Statistical Programming

  • Programming statistical analyses for IPH-sponsored clinical trials
  • Contributing to the QC of the statistical analyses realized by the other statistician(s)
  • Validating the data consistency together with the Data Manager

Methodological support

  • Contributing to the design of clinical trials, in particular the experimental plan, the endpoints, the statistical methods, the sample size needed
  • Contributing to interpreting the results and to authoring the clinical study reports

External vendor management

  • Contributing to the evaluation of the cost estimates proposed by the CROs (Contract Research Organizations)
  • Contributing to the review of the eCRF (electronic Case Report Form), edit checks, UAT (User Acceptance Tests)
  • Managing and validating the study documents (statistical analysis plan, etc.)
  • Supervising the statistical analyses carried out by the CROs

Profil

Experience and Qualifications:

  • Training in Statistics or Biostatistics (Bac+4/5, ENSAI, ISPED, INSAE, ...)
  • At least 2 years of experience in the analysis of clinical data (Biotech, Pharma company, CRO, Hospital Center, etc.)
  • Experience in Oncology (desirable)

Technical Competencies:
Essential:

  • SAS (Statistical Analysis System) programming skills
  • Knowledge of clinical trials and good clinical practices
  • Written and oral English

Desirable:

  • Knowledge of the CDISC (Clinical Data Interchange Standards Consortium) standards
  • R / R Shiny Applications
  • Knowledge of common designs in oncology

Additional Skills/ Behaviours:

  • Communication skills
  • Excellent organization and flexibility
  • Interested in multidisciplinary work and focused on team goals
  • Ability to work in an ever-evolving context, with partial information; ability to adapt and be flexible to ongoing and moving tasks

Formulaire de candidature / Application Form

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By submitting this form, I accept that the information entered will be exploited as part of my job search by any person having an interest in the study of my application within the entity in which I applied and this for the period strictly necessary for the finalization of the recruitment process and not exceeding 2 years after my application.

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