Clinical Research Associate, Oncology

Excelya>Full-time>Clinical Research Associate, Oncology

Job description

Founded in 2014, Excelya is a “people centered” contract research organization (CRO).

We offer a personal and authentic experience within an ambitious young healthcare company on its way to becoming the leader in clinical research in Europe with our 800 Excelyates. Our unique one-stop provider service model – leveraging a full-service, functional service provider and consultancy – allows our Excelyates to evolve across a wide range of projects. Working with leading experts, Excelya advances scientific, managerial and human knowledge to improve the patient journey.

For our team members, excelling with care means enjoying a challenging professional environment that encourages personal, intellectual and operational participation so that together we can be the best in our field. We are committed to empowering each Excelyate to express their natural talents, develop their full potential and invest in our unique project.

 

Mission

As part of your first mission, you will be responsible for the proper conduct of phase III clinical trials in oncology – hematology.

Your mission will be the following:

  • To select the investigating centers, to set up and follow up the clinical studies
  • Establish and monitor budgets related to clinical studies
  • Contribute to the administrative tasks required to set up and follow up the clinical studies
  • Carry out monitoring and co-monitoring visits to centers
  • Be in contact with the investigating physicians
  • Review clinical instructions as needed
  • Prepare the centers and contribute to audits and inspections
  • Ensure the traceability of any deviations encountered

Profile

  • 8 to 10 years minimum of experience in a pharmaceutical/Biotech laboratory
  • Good communicator, team player and autonomous
  • Good level of written and spoken English
  • Experience in chronic diseases (hypertension, CKD, diabetes)
  • Experience in RIPH & non-RIPH drug & medical device studies
  • Strongly valued experience in gas studies
  • Experience with data protection and patient privacy is highly valued

Summary

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