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IC
ICON plc
3d ago

Senior CRA(m/w/x)

Frankfurt am Main
Full-timeWith Home OfficeSenior

Description

You will drive the success of clinical trials by overseeing site performance and data integrity, ensuring every study meets the highest regulatory standards through expert monitoring and site support.

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Requirements

  • •Advanced degree in life sciences, nursing, or medicine
  • •Extensive experience as Clinical Research Associate
  • •Understanding of clinical trial processes and regulations
  • •Experience in Oncology
  • •Ability to manage multiple sites and projects
  • •Strong organizational and problem-solving skills
  • •Expertise in monitoring practices and site management
  • •Proficiency in clinical trial software and tools
  • •Excellent communication and stakeholder management skills
  • •Ability to influence and drive compliance
  • •Fluency in German and English
  • •Ability to travel at least 60%

Education

Master's degree

Tasks

  • •Monitor clinical trial sites for protocol adherence
  • •Ensure compliance with regulatory and GCP standards
  • •Conduct site visits to assess performance
  • •Resolve site issues and provide execution support
  • •Collaborate with teams for accurate data reporting
  • •Train and guide site staff and CRAs
  • •Maintain high standards of clinical trial conduct
  • •Build effective relationships with site personnel

Tools & Technologies

clinical trial software

Languages

German – Business Fluent

English – Business Fluent

Benefits

Healthcare & Fitness

  • •Health insurance offerings
  • •Health assessments

Retirement Plans

  • •Retirement planning offerings

Mental Health Support

  • •Global Employee Assistance Programme

Other Benefits

  • •Life assurance

Childcare

  • •Childcare vouchers

Company Bike

  • •Bike purchase schemes

Corporate Discounts

  • •Discounted gym memberships

Public Transport Subsidies

  • •Subsidised travel passes
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