CRA II - Paris

Location France
Discipline: Clinical Research
Job type: Permanent
Contact name: Grace Ticehurst

Contact email: grace.ticehurst@rbwconsulting.com
Job ref: 21439
Published: over 2 years ago
Expiry date: 26 Jul 2023 11:59

As the needs for clinical trials are rapidly increasing across Europe, one of my clients in the CRO sector are looking to once again expand their clinical team across France.

I am looking for a CRA to work on a project for a large CRO dedicated to one sponsor across, predominantly, oncology studies.

As a CRA, you will be working from home and travelling to sites localised to your region.

Responsibilities:

  • 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

Requirements:

  • Strong experience across multiple therapeutic areas
  • Previous experience working with pharmaceutical/biotech companies or CROs
  • Independent monitoring experience of a minimum of 2 years needed
  • Driving License with ability to travel to sites when needed
  • Fluent in French and English
  • Experience with regulatory and ethics submissions across clinical trials

Ideally, the client would prefer you to be working from their office in France for 2 days a week but this could potentially be negotiable depending on your experience,

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

? roxanna.keshavarz@rbwconsulting.com