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EUEurofins

Clinical Research Associate (CRA)(m/w/x)

Hamburg
Full-timeOn-siteExperienced

Monitoring clinical trials, including site selection and remote oversight, for a global lab group serving food, pharma, and consumer goods sectors. Minimum 2 years clinical monitoring experience required. Diverse project scope across food, pharma, and consumer goods.

Requirements

  • Minimum 2 years of clinical monitoring experience
  • Degree in scientific or medical discipline or equivalent
  • Very good knowledge of Good Clinical Practice/ICH Guidelines
  • Proven ability to work independently in a fast-paced environment
  • Excellent communication, interpersonal, and organizational skills
  • Fluency in German and high level of English language

Tasks

  • Act as a liaison between the sponsor, CRO, and trial site
  • Perform monitoring visits, including site selection, initiation, periodic, and close-out visits
  • Conduct remote monitoring of clinical trials
  • Generate and update monitoring plans and site initiation presentations
  • Evaluate the quality and integrity of site practices
  • Serve as a contact for clinical trial suppliers and assigned vendors
  • Identify and escalate protocol deviations and data discrepancies
  • Ensure compliance with clinical trial protocols and GCP/ICH guidelines
  • Collaborate closely with various departments at bioskin and freelance CRAs

Work Experience

  • 2 years

Education

  • Bachelor's degree

Languages

  • GermanBusiness Fluent
  • EnglishBusiness Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Eurofins 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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