Clinical Research Associate Jobs in Brandenburg, Germany

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.

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.

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

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.

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.

Associate Director, Study Site Engagement at Takeda leads local engagement with study teams, sites, and CROs. Responsibilities include supporting feasibility, site selection, and recruitment across assigned regions, coordinating pre-study visits, site initiation visits, and investigator meetings.

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.

Patient Centered Solutions (PCS) team at IQVIA drives patient‑focused research to inform clinical development and regulatory strategy. The Associate Principal/Principal leads qualitative research design, execution and AI‑enabled method innovation while mentoring staff and managing client relationships.

Clinical Research Nurse at Parexel supports clinical trials in Berlin, ensuring patient safety and accurate data collection. The role coordinates study activities, manages CRFs, and collaborates with monitors and sponsors.

Clinical Research Nurse at Parexel in Berlin supports clinical trials by delivering nursing care to study participants, ensuring safety and accurate data capture per GCP guidelines. The role coordinates study activities, prepares equipment, and collaborates with monitors and sponsors to maintain protocol compliance.

Clinical Research Coordinator at Parexel in Berlin, part of the Clinical Research Unit focused on advancing therapeutic development. The role plans, prepares, and executes Phase I‑III trials, ensuring compliance with ICH‑GCP, protocols, and SOPs, while overseeing data cleaning, deviations, and study documentation.