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ICICON plc

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

Frankfurt am Main
Full-timeRemoteExperienced

Overseeing clinical trial sites from initial qualification to final close-out for a global CRO. In-depth knowledge of clinical trial processes and ICH-GCP guidelines required. Frequent site visits across diverse locations.

Requirements

  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 2 years of experience as a Clinical Research Associate
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Strong organizational and communication skills
  • Fluency in English and German language
  • Ability to work independently and collaboratively
  • Ability to travel at least 60% of the time

Tasks

  • Conduct site qualification visits for clinical trials
  • Initiate clinical trial sites
  • Monitor clinical trial progress
  • Perform close-out visits for clinical trials
  • Ensure protocol compliance and data integrity
  • Prioritize patient safety throughout the trial process
  • Collaborate with investigators and site staff
  • Review and resolve data queries
  • Prepare and review study documentation
  • Draft clinical study reports and protocols

Work Experience

  • 2 years

Education

  • Bachelor's degree

Languages

  • EnglishBusiness Fluent
  • GermanBusiness Fluent

Benefits

More Vacation Days

  • Various annual leave entitlements

Healthcare & Fitness

  • Health insurance offerings

Retirement Plans

  • Competitive retirement planning

Mental Health Support

  • Global Employee Assistance Programme

Other Benefits

  • Life assurance

Additional Allowances

  • Flexible optional benefits
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