Senior CRA | Multi-Sponsor Trials (Home-Based Austria)

IQVIA Inc; Wien; A distancia; EUR 36.000 - 43.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Home office

Company car

Accident insurance

Pension plan

Descripción de la vacante

IQVIA in Austria is seeking a CRA or SrCRA to join our Clinical Site Management team. This home-based role covers across Austria, focusing on monitoring diverse clinical trials in collaboration with sponsors and the global study team.

You will conduct site visits, ensure GCP/ICH compliance, and manage regulatory submissions, recruitment, CRF completion, and data queries, with travel up to 70%. A strong life science background and fluent German/English are required.

Formación

• University degree in life science or healthcare apprenticeship.
• Experience as CRA, study coordinator, or clinical trial coordinator.
• Strong written and verbal communication; attention to detail.
• Fluent in German and English.
• Ability to travel up to 70%.

Responsabilidades

• Performing site selection, initiation, monitoring and close-out visits.
• Supporting the development of a subject recruitment plan.
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.
• Collaborating with experts on study sites and client representatives.

Conocimientos

Life science degree

Clinical trial experience

GCP knowledge

German and English

Driver's license

Educación

University degree in life science

Healthcare apprenticeship

Descripción del empleo

IQVIA in Austria is seeking a CRA or SrCRA to join our Clinical Site Management team. This home-based role covers across Austria, focusing on monitoring diverse clinical trials in collaboration with sponsors and the global study team.

You will conduct site visits, ensure GCP/ICH compliance, and manage regulatory submissions, recruitment, CRF completion, and data queries, with travel up to 70%. A strong life science background and fluent German/English are required.