Clinical Research Technician - German Speaking

AGATE; Düsseldorf; Vor Ort; EUR 40.000 - 65.000; Vollzeit

Zusammenfassung

Ein aufstrebendes Unternehmen im biopharmazeutischen Bereich sucht einen Clinical Research Technician, der für die Genauigkeit und Qualität von Studiendaten verantwortlich ist. In dieser Rolle arbeiten Sie eng mit einem engagierten Forschungsteam zusammen, um sicherzustellen, dass alle Daten den höchsten Standards entsprechen. Ihre Aufgaben umfassen die Datenpflege im eCRF-System Viedoc, die Einhaltung von GCP-Richtlinien und die enge Zusammenarbeit mit internen und externen Stakeholdern. Wenn Sie eine Leidenschaft für klinische Forschung haben und innovative Projekte unterstützen möchten, ist dies Ihre Chance, Teil eines dynamischen Teams zu werden.

Qualifikationen

• Mindestens 2-3 Jahre Erfahrung in der klinischen Forschung.
• Starke Erfahrung mit eCRF-Systemen, insbesondere Viedoc.

Aufgaben

• Datenmanagement für klinische Studien sicherstellen.
• Datenvalidierung und -verifizierung durchführen.

Kenntnisse

Datenmanagement

ECRF-Systeme

Gute Klinische Praxis (GCP)

Detailgenauigkeit

Organisationsfähigkeiten

Deutsch (schriftlich und mündlich)

Ausbildung

Bachelor in Lebenswissenschaften

Master in Lebenswissenschaften

Tools

Viedoc

Microsoft Excel

Microsoft Word

Microsoft PowerPoint

Jobbeschreibung

AGATE LIFE SCIENCES is a young company specialized in the biopharmaceutical industry, medical devices, and cosmetics, bringing together a community of experts passionate about innovations.

We support our large account clients in addressing scientific, technical, and operational challenges. Our team members and experts are involved in clinical operations, biometrics and data science, pharmacovigilance, regulatory affairs, and quality assurance.

We place people and the well-being of our employees at the heart of our concerns. A dynamic environment is guaranteed.

As part of a short-term mission due to business growth, we are looking for a Clinical Research Technician .

You will be responsible for ensuring the accuracy, quality, and compliance of the data entered, working closely with the research team to manage and process clinical study data.

Key Responsibilities :

• Perform accurate data entry into the Viedoc eCRF system for clinical studies.
• Ensure compliance with the study protocol, Good Clinical Practice (GCP), and regulatory requirements for data entry and management.
• Validate and verify data to ensure consistency and accuracy throughout the study.
• Identify and resolve any data discrepancies or issues in collaboration with the research team.
• Maintain detailed records of data management activities and provide status updates on data processing.
• Assist in data cleaning and preparation for analysis.
• Collaborate with internal teams and external stakeholders to ensure smooth and efficient data handling throughout the study.

Required Skills and Qualifications :

• A degree in Life Sciences, Biology, or a related field (minimum Bachelor's; Master's or specialized training in clinical research is a plus).
• At least 2-3 years of experience in a similar role, focusing on data entry and management in clinical research.
• Strong experience with eCRF systems, particularly Viedoc .
• Proficiency in German (both written and spoken) to communicate effectively with German-speaking sites and investigators.
• Knowledge of Good Clinical Practice (GCP), ICH-GCP guidelines, and data privacy regulations (e.g., GDPR).
• Strong attention to detail and organizational skills in managing large datasets.
• Proficiency in office software tools (Excel, Word, PowerPoint).

If you are passionate about clinical research and enjoy managing data for innovative projects, we would be happy to receive your application.