CRA sponsor dedicated Hamburg

Resourcing Life Science

Hamburg

Vor Ort

EUR 45.000 - 65.000

Vollzeit

14 Tage+
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Zusammenfassung

Resourcing Life Science is seeking a Clinical Research Associate (CRA) dedicated to monitoring clinical studies in Hamburg. The ideal candidate will have experience in phases II-III clinical studies, ensuring compliance with Good Clinical Practices.

This role requires a Bachelor's degree in life science and at least 1 year of relevant monitoring experience. Proficiency in both English and German is essential for effective communication.

Qualifikationen

  • Minimum 1 year monitoring experience as CRA within a CRO, Pharma, or Biotech in Germany.
  • Experience with site initiation and site close out.
  • Experience in commercial studies and clinical studies phases II-III.

Aufgaben

  • Monitor clinical studies in phases II-III.
  • Ensure adherence to Good Clinical Practices and compliance with all study procedures.
  • Identify, qualify, and initiate investigators and their sites.
  • Supervise study conduct according to GCP requirements and applicable laws.

Kenntnisse

Monitoring clinical studies
Good Clinical Practices (GCP)
Excellent communication skills
Fluent English
Fluent German

Ausbildung

Bachelor degree in life-science

Jobbeschreibung

Company Description

Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA / Clinical Research Associate sponsor dedicated in Hamburg.

Job Overview
  • Monitoring clinical studies in phases II-III
  • Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.
  • Identification, qualification and initiation of investigators and their sites.
  • Supervising study conduct according to GCP requirements and all applicable laws.
Key Requirements
  • Bachelor degree in life-science
  • Min 1 year monitoring experience as CRA within a CRO, Pharma, Biotech in Germany
  • Experience in commercial studies
  • Experience with site initiation, site close out
  • Experience in clinical studies phase II-III
  • Fluent English & German
  • Excellent communication skills
  • A full clean driver's license
  • FTE: 1.0
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