Senior Biostatistician

Excelya>All job opportunites>Senior Biostatistician

Job description

Senior Biostatistician

Posted on : September 15th

Excelya, one of the leading independent CRO in Europe.

Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care.

We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 800 Excelyates. Our unique one-stop provider service model – leveraging full-service, functional service provider and consulting – allows our Excelyates to evolve through a diverse array of projects. In collaboration with preeminent experts, Excelya advances scientific, managerial and human knowledge to improve the patient journey.

For our team members, excelling with care means benefitting from a stimulating professional environment that encourages personal, intellectual, and operational participation so that together we can be the best in our field. We commit to giving each Excelyate the means to express their natural talents, develop their full potential and invest their unique selves in our unique project.

To learn more about us, visit



The purpose of the mission is to contribute to the implementation and monitoring of clinical trials in collaboration with the project manager statistician and the clinical team, so that the statistical analyses meet the primary and secondary objectives of the study while respecting the deadlines, quality, regulatory requirements, and guidelines of the pharmaceutical laboratory.

Participate in study design, establish sample size, and even develop simulation pro-grams to evaluate the operational characteristics of a trial.

Review and contribute to the drafting of study documents: Case Report From (CRF), Central monitoring Plan (CMP), Study Risk Management Plan, IRT specifications….

Determine the randomisation scheme and ensure that it is carried out correctly by the IRT
Define the specifications of the subcontracting to the CRO in charge of the study and the technical specifications given to this CRO

Write a precise, clear, and complete statistical analysis plan (SAP) with the most ap-propriate methodology and data presentation. Construct the list of statistical appendices for the study.
In the case of a study subcontracted to a CRO, proofread, and validate the statistical analysis plan (SAP)

Supervise the subcontracted biostatistical and programming activity (including data monitoring, preparation of ADS and report tables)

Verify CRO deliverables
Validate SDTM/ADAM documentation (mainly derived variables)

Communicate, discuss, and interpret statistical results, including joint development of the clinical study report

Participate in submission activities


You have a Master degree/engineering school (ENSAI, ISPED…)

You have at least 5 years of experience in the pharmaceutical industry

A good knowledge of statistical methods is essential

Significant experience in interventional phases and in oncology

Professional English (written/oral) required
The position can be done by telecommuting in France.

The position can be done by telecommuting in France.

If you want to join an attractive CRO which develops and retains talents, don’t hesitate and join us!



Apply for this job

Similar career opportunities

Clinical Research Associate

  • France
  • September 15, 2021

FSP Line Manager

  • France
  • September 15, 2021

Trial Support Operation Manager

  • France
  • September 15, 2021