Clinical Research Associate Jobs in Saarland, Germany

Clinical Research Associate (CRA) (m/w/d) – Zelltherapie (Außendienst) at AstraZeneca is part of the Site Management & Monitoring team, driving the monitoring of cell therapy trials such as CAR‑T, TCR‑T and Treg. The role involves on‑site monitoring visits, data quality oversight, and collaboration with international study teams to ensure timely, compliant study conduct.

AstraZeneca’s Site Management & Monitoring team drives clinical trials for cutting‑edge cell therapies such as CAR‑T, TCR‑T and Treg. The CRA monitors study sites, ensures timely data capture, and collaborates with investigators across Germany.

Site Management & Monitoring team at AstraZeneca drives clinical trials in cell therapy (CAR‑T, TCR‑T, Treg). The CRA monitors sites, ensures data quality, and supports recruitment and training across Germany.

Innovativ, dynamisch und nachhaltig: Als eines der weltweit führenden Unternehmen der forschenden Arzneimittelindustrie bieten wir bei AstraZeneca die besten Möglichkeiten für Ihre persönliche und berufliche Entwicklung. Für uns steht fest: Forschung bildet das Fundament unserer aller Zukunft.

Innovativ, dynamisch und nachhaltig: Als eines der weltweit führenden Unternehmen der forschenden Arzneimittelindustrie bieten wir bei AstraZeneca die besten Möglichkeiten für Ihre persönliche und berufliche Entwicklung. Für uns steht fest: Forschung bildet das Fundament unserer aller Zukunft.

Innovativ, dynamisch und nachhaltig: Als eines der weltweit führenden Unternehmen der forschenden Arzneimittelindustrie bieten wir bei AstraZeneca die besten Möglichkeiten für Ihre persönliche und berufliche Entwicklung. Für uns steht fest: Forschung bildet das Fundament unserer aller Zukunft.

BeOne Medicines I GmbH’s Clinical Research Associate team drives oncology and onco‑hematology trials, ensuring GCP compliance and site performance. The role monitors sites, manages data quality, and collaborates with regional study teams to meet milestones.

Clinical Research Associate I or II at Fortrea Germany GmbH, a team focused on delivering high‑quality clinical trials across oncology, dermatology, respiratory, cardiology, and diabetes. The role supports site management, monitoring, SDV, documentation, and IP tracking while collaborating with cross‑functional teams.

BeOne Medicines I GmbH’s Clinical Research Associate team drives oncology trial excellence by monitoring sites, ensuring GCP compliance, and managing data quality. The role conducts site selection, initiation, routine and closeout visits, documents findings, and collaborates with regional study managers to meet milestones.

Merck’s Animal Health R&D team in Schwabenheim seeks a Clinical Research Associate to conduct and monitor veterinary clinical studies, manage logistics, and ensure compliance with GCP and GMP. The role involves protocol training, data entry oversight, and collaboration with sites across Germany and Europe. Hybrid work model with on-site presence in Schwabenheim and up to 30% travel.

Clinical Research Associate team at IQVIA France drives oncology clinical trials by conducting site monitoring visits, administering protocol training, and ensuring GCP compliance. The role manages study progress, maintains TMF/ISF, generates visit reports, and collaborates with cross-functional teams to resolve data queries.

Clinical Research Associate at IQVIA’s France RDS team, responsible for monitoring oncology clinical trials across multiple sponsors. Day‑to‑day duties include site visits, training delivery, compliance oversight, and data query resolution to ensure protocol integrity.

ProPharma seeks a Serbian-speaking Clinical Research Associate for an 18‑month fixed‑term contract. Responsible for monitoring clinical sites in person and remotely, conducting study start‑ups, developing monitoring documentation, reviewing source documents and case reports, managing investigational supplies, monitoring enrollment and adverse events, reviewing regulatory documents, communicating with site personnel and cross‑functional teams, and participating in project meetings.

Cardiac Management Solutions division of ZOLL Medical develops life‑saving cardiac devices such as the LifeVest wearable defibrillator. The Clinical Research Associate supports EMEA clinical trials, managing site monitoring, regulatory documentation, and cross‑functional coordination to ensure protocol compliance and data quality.

Novotech’s Clinical Research Associate team safeguards trial participant rights and ensures data integrity across global studies. The role manages site relationships, monitors compliance with ICH GCP and local regulations, and coordinates recruitment and data verification.

Seeking experienced Clinical Research Associates to manage multi-site studies in Belgium, focusing on medical devices. Responsibilities include site monitoring, performance oversight, and ensuring high-quality deliverables while traveling 50‑80% of the time.

Sponsor Dedicated Clinical Research Team at IQVIA focuses on delivering high‑quality clinical trial monitoring for pharmaceutical sponsors. The Clinical Research Associate II conducts site initiation, monitoring and close‑out visits, manages recruitment plans, ensures regulatory compliance, and collaborates with global project teams.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Clinical Research Associate monitors sites, conducts qualification, initiation, interim and close‑out visits, ensures protocol adherence, and verifies data integrity.

Experienced Clinical Research Associate with a university degree in a scientific discipline and extensive experience in the pharmaceutical and clinical trials industry. Skilled in site monitoring, Good Clinical Practice, and International Conference on Harmonization guidelines, I manage study progress, regulatory submissions, recruitment, and data quality.

Clinical Research team at Merck Animal Health conducts field studies across Europe to develop veterinary products. The Clinical Research Associate independently manages site visits, documentation, data verification and logistics, ensuring compliance with GCP and VICH guidelines.