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ICICON plc

Senior CRA (Sponsor Dedicated)(m/w/x)

Frankfurt am Main
Full-timeWith Home OfficeSenior

Monitoring clinical trial sites at a global clinical research organization for a dedicated sponsor, ensuring protocol adherence. Extensive CRA experience managing multiple sites and projects required. Direct engagement with a single dedicated sponsor.

Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive experience as a Clinical Research Associate
  • Proven ability to manage multiple sites and projects
  • Expertise in monitoring practices and data integrity
  • Excellent communication skills in German and English
  • Ability to travel at least 60% of the time

Tasks

  • Monitor clinical trial sites for protocol adherence
  • Conduct site visits to assess performance and resolve issues
  • Collaborate with teams for accurate data collection and reporting
  • Provide training and guidance to site staff and CRAs
  • Build and maintain relationships with site personnel and stakeholders

Work Experience

  • approx. 4 - 6 years

Education

  • Master's degree

Languages

  • GermanBusiness Fluent
  • EnglishBusiness Fluent

Benefits

More Vacation Days

  • Various annual leave entitlements

Healthcare & Fitness

  • Health insurance offerings

Retirement Plans

  • Retirement planning offerings

Mental Health Support

  • Global Employee Assistance Programme

Other Benefits

  • Life assurance
  • Flexible optional benefits
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.

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