Clinical Research Associate – Hybrid (Germany)

CTI

France

Sur place

EUR 52 000 - 80 000

Plein temps

14 jours+

Générateur de candidature

Une candidature sur mesure pour ce poste — un CV personnalisé et une lettre de motivation qui correspondent directement à l’offre.

Passez les filtres ATS

Résumé du poste

CTI is seeking a Clinical Research professional to serve as the main contact for assigned study sites and to conduct site visits across pre-study, initiation, interim monitoring, and close-out phases in compliance with ICH GCP. You will support start-up activities, site selection, and regulatory document handling while maintaining timelines.

The role requires 3–5 years of CRA experience, including independent monitoring in Germany, a life science background, and fluent English (B2).

Qualifications

3–5 years clinical research experience as a CRA or related role, including independent monitoring in Germany.
Life science background.
Strong knowledge of ICH-GCP and regulatory requirements.
Fluent English (minimum Level B2) in speaking and writing.

Responsabilités

Serve as main CTI contact for assigned study sites and manage monitoring visits.
Conduct PSV, SIV, IMV, and COV with quality and timelines per Monitoring Plan.
Assist with or oversee start-up activities, feasibility, and site selection.
Collect, review and track essential regulatory documents.
Perform site management activities and report site status to the Clinical Project Manager.
Conduct remote monitoring per Monitoring Plan.
Utilize systems and reports to track subject status, SDV, and IP.
Participate in project team meetings and contribute to activities.