Clinical Research Associate Jobs in Saxony-Anhalt, 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) – 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.

Research and Development team at AbbVie drives innovative medicines through clinical trials. As a Clinical Research Associate II you will manage study sites, monitor compliance, and coordinate with local CRA colleagues to ensure timely project execution across Germany.

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, and ensures protocol compliance and data integrity.

Clinical Operations team at Linical conducts clinical trials across therapeutic areas. The Clinical Research Associate ensures site feasibility, initiation, monitoring, and close-out, handling regulatory compliance, data integrity, and investigational product management.

Experienced Clinical Research Associate (CRA) sought for leading CRO ClinChoice in Germany. The role blends global CRO stability with direct sponsor collaboration, focusing on medical device trials.

Clinical Operations at TFS HealthScience drives the execution of Phase II and III oncology trials across Europe. The Clinical Research Associate independently plans, conducts, and follows up on site initiation, monitoring, and close‑out visits, reviews eCRF data, ensures regulatory compliance, and collaborates with medical, project management, quality, and data teams.

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.

Clinical Research team at ProPharma Group provides regulatory and monitoring expertise for biotech and pharma drug development. The Senior Clinical Research Associate conducts site monitoring, initiates studies, manages documentation, and ensures compliance with GCP and local regulations.

Clinical Services – Clinical Study Delivery team at Alimentiv oversees clinical site monitoring and management for multinational studies. The Senior Clinical Research Associate leads monitoring activities, mentors CRAs, coordinates site recruitment, ensures compliance, and acts as primary liaison with sponsors.

Parexel FSP is expanding its oncology clinical research team to support a key sponsor. The Senior Clinical Research Associate will manage site activation, monitoring, and close‑out for clinical trials, ensure compliance with GCP and local regulations, and coordinate safety reporting and audit activities.

Senior Clinical Research Associate at Parexel responsible for site management, monitoring, and close‑out of clinical trials in the EU. Ensures compliance with GCP, ICH, FDA, and local regulations, manages timelines, coordinates with study teams, vendors, and safety units, and serves as audit point of contact. Requires a bachelor’s in life sciences, 3.5+ years of site monitoring experience (preferably oncology), and knowledge of oncology, vaccines, internal medicine or infectious diseases.

Clinical Research Associate I/II, FSP at Thermo Fisher Scientific works within the global clinical monitoring team to ensure oncology and cell therapy trials meet protocol, ICH‑GCP and regulatory standards. The role conducts remote and on‑site site visits, performs risk‑based monitoring, data verification and documentation, and collaborates with investigators and the project team to resolve findings.

EPCU at Parexel in Berlin seeks an Associate Clinical Research Physician to co‑investigate Phase I/II trials, ensuring participant safety and supporting the Principal Investigator with trial preparation, conduct, and reporting. The role involves 32 hours per week, morning/afternoon shifts with occasional nights and weekends as needed.

Clinical Payments Team supports financial transactions for clinical research sites, sponsors, and internal stakeholders. The Associate monitors tickets, prepares payment confirmations, maintains records, and assists with system migrations and study reconciliations.