CRA I/II — Home-Based in Austria (Single Sponsor)

IQVIA

United States

Remote

USD 39,000 - 47,000

Full time

14 days+
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Benefits offered by this job

Home office
Company car
Accident insurance

Job summary

IQVIA is seeking a Clinical Research Associate I or II (m/w/d) to work home-based across Austria in our single sponsor department. You will gain direct exposure to client teams and a broad range of therapeutic areas while benefiting from world-class training and mentoring.

You’ll perform site visits, support recruitment planning, ensure GCP/ICH compliance, manage regulatory submissions and data queries, and collaborate with study sites. Travel up to 40-60% may be required.

Qualifications

  • University degree in life science or health care field.
  • At least one year of on-site monitoring experience.
  • Knowledge of GCP/ICH guidelines.
  • Fluency in German (C1) and good command of English.
  • Driver’s license class B.

Responsibilities

  • Performing site selection, initiation, monitoring and close-out visits.
  • Supporting the development of a subject recruitment plan.
  • Evaluating site practices for compliance with GCP/ICH guidelines.
  • Managing regulatory submissions, recruitment, CRF completion, and data query resolution.
  • Collaborating with study sites and client representatives.
  • Remote monitoring, study start-up involvement, or therapeutic-area specialization as applicable.
  • Mentoring less experienced team members and providing subject matter support.

Skills

German fluency
English proficiency
Communication skills
Attention to detail

Education

Life science degree or healthcare apprenticeship

Job description

IQVIA is seeking a Clinical Research Associate I or II (m/w/d) to work home-based across Austria in our single sponsor department. You will gain direct exposure to client teams and a broad range of therapeutic areas while benefiting from world-class training and mentoring.

You’ll perform site visits, support recruitment planning, ensure GCP/ICH compliance, manage regulatory submissions and data queries, and collaborate with study sites. Travel up to 40-60% may be required.

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