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IQIQVIA

Clinical Research Associate 1 or 2 Single Sponsor(m/w/x)

Frankfurt am Main
Full-timeRemoteJunior

On-site monitoring and close-out visits for clinical trials at a global CRO. Subject recruitment planning and GCP compliance evaluation required. Home-office, company car, and flexible schedules.

Requirements

  • University degree in life science or scientific discipline, or healthcare apprenticeship
  • Minimum 12 months on-site monitoring experience
  • Knowledge of GCP and ICH guidelines
  • Strong written and verbal communication skills
  • Attention to detail
  • Ability to work in fast-paced environment
  • German fluency at C1 level
  • Good command of English
  • Flexibility for travel up to 40-60%
  • Driver's license class B

Tasks

  • Conduct site selection, initiation, monitoring, and close-out visits
  • Develop a subject recruitment plan
  • Evaluate site practices for compliance with GCP and ICH guidelines
  • Track regulatory submissions, recruitment, CRF completion, and data query resolution
  • Collaborate with study site experts and client representatives
  • Participate in remote monitoring and study start-up processes
  • Specialize in therapeutic areas, including pharmaceutical products or medical devices
  • Mentor less experienced team members
  • Provide expertise on specific topics or additional tasks

Work Experience

  • 1 year

Education

  • Vocational certificationOR
  • Bachelor's degree

Languages

  • GermanBusiness Fluent
  • EnglishBusiness Fluent

Benefits

Flexible Working

  • Home-office
  • Flexible working schedules

Company Vehicle

  • Company car or car allowance

Other Benefits

  • Accident insurance

Retirement Plans

  • Pension

Career Advancement

  • Career growth resources

Startup Environment

  • Dynamic work environments
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