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
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