Senior Clinical Research Associate - south Germany

Resourcing Group; Deutschland; Vor Ort; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

Resourcing Group currently seeks a Clinical Research Associate to monitor trials in phases II-III across sites in Germany. You will ensure compliance with GCP, investigator integrity, and study procedures, coordinating with trial sites and sponsors to maintain data quality and patient safety.

The role requires a life-science degree and at least 1.5 years of CRA monitoring experience in CRO/pharma/biotech, with hands-on site initiation and close-out.

Qualifikationen

• Bachelor degree in life-science required.
• Minimum 1.5 years of monitoring experience as CRA in CRO/pharma/biotech.
• Experience with site initiation and site close-out.
• Experience in clinical studies phase II–III.

Aufgaben

• Monitor clinical studies in phases II-III according to GCP.
• Assure adherence to GCP, investigator integrity, and study procedures.
• Identify, qualify, and initiate investigators and sites.
• Supervise study conduct in compliance with laws and guidelines.

Kenntnisse

Clinical research monitoring

Ausbildung

Bachelor's degree in life-science

Jobbeschreibung

• 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 1.5 year monitoring experience as CRA within a CRO, Pharma, Biotech
• Experience in commercial studies
• Experience with site initiation, site close out
• Experience in clinical studies phase II-III