​Freelance CRA

Discipline: Clinical Research
Job type: Contract
Salary: £Day / Hourly Rate: On application
Contact name: Roxanna Keshavarz

Contact email: Roxanna.Keshavarz@rbwconsulting.com
Contact phone: 01293584300
Job ref: 21113(RK)
Published: over 4 years ago
Expiry date: 30 Apr 2021 11:59

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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

  • Assist in the preparation and management of regulatory and ethics applications for clinical research studies as required

  • Ensure that all adverse events are reported in accordance with the required time frames for reportability

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Requirements:

  • Previous experience working with pharmaceutical/biotech companies or CROs

  • Independent monitoring experience of a minimum of 2 years’

  • Fluent in English, German and Italian

  • Worked as a freelancer for a minimum of 1 year

  • 0.5-0.6 FTE available

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If you are interested in discussing this role in further detail, you can reach me on: +44 1273 952187 / roxanna.keshavarz@rbwconsulting.com

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Day / Hourly Rate: On application