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ICICON plc

(Senior) Clinical Research Associate (CRA) - sponsor dedicated(m/w/x)

Frankfurt am Main
Full-timeRemote

Coordinating clinical study setup and monitoring activities for a specific pharmaceutical client. 60% travel and ICH-GCP knowledge required. Consistent client focus due to dedicated role.

Requirements

  • University degree in medicine, science, or equivalent
  • Knowledge of ICH-GCP guidelines and medical data expertise
  • Excellent written and verbal English and German
  • Good social skills and timely query management
  • Ability 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 and monitor study cost efficiency
  • Prepare and review study documentation
  • Conduct feasibility studies for new proposals
  • Build collaborative relationships with clinical investigators
  • Maintain strong connections with site staff
  • Ensure patient safety through protocol compliance
  • Adhere to regulatory requirements and procedures

Education

  • Bachelor's degree

Languages

  • EnglishBusiness Fluent
  • GermanBusiness Fluent

Tools & Technologies

  • ICH-GCP guidelines

Benefits

More Vacation Days

  • Various annual leave entitlements

Healthcare & Fitness

  • Range of health insurance
  • Health assessments

Retirement Plans

  • Competitive retirement planning

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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