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ICICON plc

CRA I (sponsor dedicated)(m/w/x)

Frankfurt am Main
Full-timeWith Home OfficeExperienced

Clinical study setup and monitoring, including documentation and query resolution, for a specific pharmaceutical client at a healthcare intelligence CRO. University degree in medicine or science, with ICH-GCP knowledge and 60% travel willingness required. Single-client focus with close collaboration.

Requirements

  • University degree in medicine, science, or equivalent
  • Knowledge of ICH-GCP guidelines and medical data evaluation
  • Excellent written and verbal English and German
  • Good social skills and timely query management
  • Willingness to travel 60% and valid drivers license

Tasks

  • Coordinate all study setup and monitoring activities
  • Complete accurate study status reports
  • Maintain comprehensive study documentation
  • Resolve sponsor-generated queries efficiently
  • Manage study cost efficiency
  • Prepare and review study documentation
  • Conduct feasibility studies for new proposals
  • Develop collaborative relationships with clinical investigators and site staff
  • Ensure patient safety through protocol and regulatory compliance

Work Experience

  • approx. 1 - 4 years

Education

  • Bachelor's degree

Languages

  • EnglishBusiness Fluent
  • GermanBusiness Fluent

Tools & Technologies

  • ICH-GCP guidelines

Benefits

Healthcare & Fitness

  • Health insurance offerings
  • Health assessments

Retirement Plans

  • Competitive retirement planning

Mental Health Support

  • Global Employee Assistance Programme

Other Benefits

  • Life assurance
  • Reasonable accommodations

Childcare

  • Childcare vouchers

Company Bike

  • Bike purchase schemes

Corporate Discounts

  • Discounted gym memberships

Public Transport Subsidies

  • Subsidised travel passes

Informal Culture

  • Inclusive and accessible environment
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