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IQIQVIA Biotech

Clinical Research Associate 2(m/w/x)

Frankfurt am Main, München, Hamburg
Full-timeRemoteExperienced

Conducting site visits for clinical trials, supporting subject recruitment plans for medical treatments. Two years of on-site monitoring experience and GCP/ICH knowledge required. Company car, home-office, flexible schedules.

Requirements

  • University Degree in life science or other scientific discipline or apprenticeship in the health care field
  • Minimum two years of on-site monitoring experience or equivalent combination of education, training and experience
  • Knowledge of clinical research regulatory requirements (GCP, ICH guidelines)
  • Strong written and verbal communication skills
  • Attention to detail
  • Ability to work in a fast-paced environment
  • Flexibility for business travel (40-60%)
  • Driver’s license class B

Tasks

  • Conduct site selection visits
  • Conduct site initiation visits
  • Conduct site monitoring visits
  • Conduct site close-out visits
  • Support the development of subject recruitment plans
  • Evaluate site practices for quality and integrity
  • Ensure compliance with GCP and ICH guidelines
  • Track regulatory submissions
  • Monitor recruitment progress
  • Oversee case report form (CRF) completion
  • Track data query resolution
  • Collaborate with study site experts and client representatives
  • Mentor less experienced team members
  • Provide subject matter expertise on specific topics

Work Experience

  • 2 years

Education

  • Vocational certificationOR
  • Bachelor's degree

Languages

  • GermanBusiness Fluent
  • EnglishBusiness Fluent

Benefits

Flexible Working

  • Home-Office
  • Flexible work schedules

Company Vehicle

  • Company car

Other Benefits

  • Accident insurance

Career Advancement

  • Career growth resources
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