Share this Job

Guerbet is a leader in medical imaging worldwide, offering a wide range of pharmaceutical products, medical devices, digital and AI solutions for diagnostic and interventional imaging, to improve the diagnosis and treatment of patients.

A pioneer since more than 90 years in the field of contrast media, Guerbet is continuously innovating with 9% of revenue dedicated to Research & Development and four centers in France, Israel and the United States.

Guerbet (GBT) is listed on Euronext Paris (segment B – mid caps) and generated €817 million in revenue in 2019 with a global workforce of over 2,800 employees.

Achieve, Cooperate, Care and Innovate are the values that Guerbet's employees share and practice every day. Working at Guerbet means playing a unique part in the future of medical imaging. Passionate about its business, the company strive day in, day out to combine performance, quality and sustainable development.

For more information about Guerbet, please go to www.guerbet.com  and follow Guerbet on Twitter @GuerbetGroup


Statistician - Clinical Trials M/F (Permanent)

Location : Villepinte (93), Ile-de-France



We are looking for an exprienced Statistician M/F who will be a part of our Medical Affairs & Clinical Development teams based in Guerbet Headquarters.You will be responsible to plan and execute statistical analyses of all Guerbet sponsored clinical trials from Phase I to IV for both pharmaceutical products and medical devices.


You will interpret data and communicate results to the project teams and other stakeholders. In this role you'll ensure that complex statistical concepts are explained in a way that the project teams can understand and advise on strategy.




Main responsibilities (but not limited):


  • Support to define what data to collect and how it should be gathered
  • Take into account any ethical and legislative considerations in data collection
  • Design clinical trials or surveys to produce the required data
  • Collecting and analyze the data, interpreting the data
  • Help ensuring that the right decisions are made based on the results
  • Monitor data collected throughout the life cycle of the products in the portfolio of the company
  • Present results to the project teams and other stakeholders, such as senior managers, regulatory authorities, etc
  • Supporting for clinical studies reports and articles for publication




More than your skills, your personality and your potential will make the difference: Analytical and problem-solving oriented, you have good teamwork and collaborative skills


Desired skills and background:


  • Holder of Bachelor or Master's degree in biostatistics/mathematics/bioinformatics or equivalent
  • At least 5 years’ experience in pharmaceutical, medical device industry or CRO 
  • Strong mathematics abilities with wide-ranging computer skills
  • A knowledge with SAS programming and CDISC competence
  • Ability to communicate findings to non-statisticians
  • Fluent in English