Clinical Research Associate Jobs in Hamburg, Germany

Clinical Research Associate (CRA) (m/w/d) – Onkologie (field‑based) at AstraZeneca. Responsible for monitoring oncology clinical trials across Berlin, Magdeburg, Leipzig, Dresden.

Clinical Research Associate (CRA) (m/w/d) – Region Mitteldeutschland/Raum Frankfurt at AstraZeneca. The role is field‑based and permanent, focusing on monitoring clinical trials across immunology, respiratory, metabolic and cardiovascular indications.

Clinical Research Associate (CRA) – Onkologie – responsible for monitoring oncology clinical trials across Eastern and Southern Germany, ensuring accurate, timely data collection and compliance with ICH‑GCP, AMG and other regulations. Duties include feasibility assessment, site initiation, recruitment, ongoing monitoring, database lock, closure, and reporting.

The Clinical Research Associate (CRA) at Eurofins Bioskin bridges sponsors, CROs, and trial sites, ensuring high-quality clinical trials in dermatology. The role involves site selection, initiation, periodic and close‑out visits, remote monitoring, and continuous quality control.

Clinical Research Associate (CRA) – Field-based position at AstraZeneca in Hamburg. The role focuses on site management and monitoring of clinical trials in cell therapy, including CAR‑T, TCR‑T, and Treg indications across phases I‑III.

Cell Therapy Site Management & Monitoring at AstraZeneca drives clinical studies for innovative cell therapies such as CAR‑T and TCR‑T. The Clinical Research Associate monitors studies across all phases, ensures data quality, conducts site visits, and supports investigators while traveling throughout Germany.

Cell Therapy Site Management & Monitoring at AstraZeneca drives the execution of clinical studies for innovative cell therapies such as CAR‑T, TCR‑T and Treg. The CRA monitors study sites across all phases, ensures high‑quality data capture, conducts risk‑based and remote monitoring, and supports site initiation and training.

Cell Therapy Site Management & Monitoring at AstraZeneca drives clinical studies for innovative cell therapies such as CAR‑T, TCR‑T and Treg. The CRA monitors studies across all phases, ensures high‑quality data capture, conducts site visits, supports site initiation and training, and escalates issues to study leadership.

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.

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.

Biorasi seeks a Senior Clinical Research Associate to oversee site visits, regulatory tracking, and data management across clinical trials in Denmark. The role involves planning and executing site selection, initiation, interim, and close‑out visits, drafting reports, managing investigational product logistics, and ensuring compliance with ICH GCP and local regulations.

SRS FSP team at TFS HealthScience, a global CRO, drives clinical trial monitoring and site management. The Lead Clinical Research Associate oversees monitoring strategy for Phase I/II studies, leads CRAs, ensures GCP compliance, and drives risk‑based monitoring.

IQVIA’s Clinical Research Associate team in Copenhagen drives site monitoring and management to ensure compliance with GCP and ICH guidelines. The role conducts initiation, monitoring, and close‑out visits, manages recruitment plans, and maintains Trial Master File documentation.

CRA Manager at Merck leads a Danish Clinical Research Associate team of up to 15 members, driving high‑quality trial oversight and compliance with ICH GCP, local regulations, and company standards. The role reports directly to the Head of Site Management & Monitoring and is a key country‑level leadership position within Global Clinical Trial Operations.

Genmab seeks an Associate Director, Clinical Research Scientist to lead or co‑lead complex clinical trials, develop program strategy, author regulatory documents, and provide medical input for site selection and data review.