Clinical Research Associate — Growth & Global Trials

Fortrea

Wien

Vor Ort

EUR 42.000 - 62.000

Vollzeit

vor 23 Stunden
Sei unter den ersten Bewerbenden
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Eine komplette Bewerbung in einer Minute — maßgeschneiderter Lebenslauf und Anschreiben, versandbereit.

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Zusammenfassung

Fortrea is seeking a Clinical Research Associate to advance from onsite monitoring to broader clinical trial delivery. The role emphasizes supporting sites, maintaining documentation, and ensuring patient safety under supervision.

The ideal candidate has at least 1 year of onsite monitoring experience, a life sciences degree, and fluency in German and English. Travel for site visits is expected, with opportunities for professional development in a structured environment.

Qualifikationen

  • University or college degree in life sciences, nursing, pharmacy, or a related field; relevant internships or equivalent experience will be considered.
  • Minimum of 12 months of onsite monitoring experience
  • Basic understanding of ICH‑GCP guidelines and clinical trial processes.
  • Strong attention to detail, willingness to learn, and ability to follow established procedures and documentation standards.
  • Fluency in German and English, both written and spoken.
  • Comfortable using clinical systems and tools, with openness to travel as required for site visits.

Aufgaben

  • Support the management of clinical trial sites in compliance with Fortrea SOPs, ICH‑GCP, study protocols, and sponsor requirements, with appropriate supervision.
  • Assist in the preparation and conduct of site monitoring activities, including site initiation, routine monitoring, and close‑out visits, ensuring patient safety and protocol adherence.
  • Perform source data verification (SDV), support query resolution, and review eCRFs to help ensure data quality and completeness.
  • Maintain and update essential trial documentation in eTMF and sponsor systems to support inspection readiness.
  • Support investigational product (IP) tracking and accountability checks in collaboration with the study team.
  • Collaborate with cross‑functional teams and elevate issues appropriately, contributing to site performance, quality, and timelines.

Kenntnisse

Onsite monitoring
ICH-GCP knowledge
Attention to detail
German language
English language
Willingness to travel

Ausbildung

Life sciences degree

Jobbeschreibung

Fortrea is seeking a Clinical Research Associate to advance from onsite monitoring to broader clinical trial delivery. The role emphasizes supporting sites, maintaining documentation, and ensuring patient safety under supervision.

The ideal candidate has at least 1 year of onsite monitoring experience, a life sciences degree, and fluency in German and English. Travel for site visits is expected, with opportunities for professional development in a structured environment.

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