Location Paris
Discipline: Clinical Research
Job type: Permanent
Salary: £Salary: On application
Contact name: Roxanna Keshavarz

Contact email:
Contact phone: 01293584300
Job ref: 20916
Published: about 1 month ago
Expiry date: 11 April 2021


  • Perform on-site monitoring visits as well as site identification, feasibility and selection as required

  • Prepare project-specific support materials and templates in accordance with protocol and other specifications

  • Manage the content of project site-level Trial Master Files and ensure accuracy and completeness

  • Assist in the preparation and management of regulatory and ethics applications for clinical research studies as required


  • Strong experience across Oncology

  • Previous experience working with pharmaceutical/biotech companies or CROs

  • Independent monitoring experience of a minimum of 2 years needed

  • Driving Licence with ability to travel to sites when needed

  • Fluent in French and English

  • Experience with regulatory and ethics submissions across clinical trials

This position will be client office based in France with 2 home based days per week.
If you’re interested in this role, please get in touch and I will be happy to discuss this in further detail: +44 1273 952187

Salary: On application