Senior Clinical Research Associate

Senior Clinical Research Associate

Competitive salary

Spain

My client is a mid-sized CRO and due to a number of extra projects in which they have taken on, starting this year, they are rapidly looking to expand their clinical team across Europe with a number a different levelled CRAs.

Responsibilities:

• Perform on-site monitoring visits as well as site identification, feasibility and selection as required
• Responsible for evaluating, initiating, monitoring and closing out clinical study sites
• Ensure clinical projects are conducted, recorded, and reported in accordance with the project protocol
• Comply with Good Clinical Practice (GCP), Company SOPs and all applicable regulatory requirements
• Provide ongoing updates and support to project management

Requirements:

• At least 2 years of experience with independent monitoring in Spain
• Previous CRO experience
• Excellent knowledge of ICH-GCP and any other relevant, local regulatory requirements
• Ability to travel 25% of the time
• Fluent in English and Spanish

If you’re interested in a new challenge for the new year, then get in touch today to discuss this role in further details:

+44 1273 952187

roxanna.keshavarz@rbwconsulting.com