CRA II / Senior Clinical Research Associate

I am working with a large CRO which is looking for a CRA II / Senior Clinical Research Associate to expand their Oncology team in Italy.

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Responsibilities:

• Perform on-site monitoring visits as well as site qualification, site initiation, 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 ICH-GCP), company SOPs/processes, protocol compliance and all applicable regulatory requirements

• Provide ongoing updates and support to project management

• Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions

• Demonstrates diligence in protecting the confidentiality of each subject/patient

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Requirements:

• Bachelor’s degree in related field

• At least 3 years of experience as a Clinical Research Associate

• Strong background in Oncology

• Excellent knowledge of ICH-GCP and any other relevant, local regulatory requirements

• Ability to travel 50% of the time

• Fluent in English and Italian

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If you’re interested in this role, please get in touch and I will be happy to discuss this in further detail, you can reach me on: roxanna.keshavarz@rbwconuslting.com / +44 1273 952187

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Salary: On application