Clinical Research Associate – Germany

Resourcing Life Science

Deutschland

Vor Ort

EUR 55.000 - 70.000

Vollzeit

14 Tage+
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Zusammenfassung

Resourcing Life Science is seeking a CRA in Germany to monitor clinical studies in phases II-III for a Global CRO partner.

You will ensure adherence to GCP, identify and initiate investigators and sites, and supervise study conduct in line with regulatory requirements.

The role requires fluency in English and German, a full driving license, and the ability to work independently within cross-functional teams.

Qualifikationen

  • 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 drivers license
  • FTE: 1.0

Aufgaben

  • 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.

Kenntnisse

Fluent English
Fluent German
Excellent communication skills
Driver's license

Ausbildung

Bachelor's 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 in Germany

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 drivers license
  • FTE: 1.0
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