Clinical Research Associate Jobs in Mecklenburg-Vorpommern, 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.

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) – 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.

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) – Onkologie (field‑based) at AstraZeneca. Responsible for monitoring oncology clinical trials across Berlin, Magdeburg, Leipzig, Dresden.

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.

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.

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.

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.

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.

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.

Genmab, a Danish biotechnology company, seeks an Associate Director, Clinical Research Scientist to lead or co‑lead complex clinical trials for antibody therapeutics. The role involves developing program strategy, authoring clinical and regulatory documents, overseeing data review, providing medical input for site selection, coordinating committees, preparing presentations, and contributing to publications.