Junior Clinical Research Associate

​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

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Requirements:

• Monitoring experience across Germany with 1-2 years' experience of independently monitoring

• Fluent in English and German

• Driving License with ability to travel 50% of the time

• Worked as a SCRA for at least 2 years

• Has a suitable home office to work from

• Experience working with CROs

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

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Salary: On application