Clinical Research Associate Jobs in Lower Saxony, Germany

Clinical Operations at BeOne Medicines drives oncology clinical trials from start-up to closeout. The Clinical Research Associate monitors trial sites, ensures compliance with ICH/GCP, and collaborates with the Regional Clinical Operations Manager to meet study timelines and quality standards.

Premier Research is hiring a Clinical Research Associate II to join the Clinical Monitoring, Site Management and SSU team in Germany. The role supports biotech, medtech, and specialty pharma companies by monitoring clinical studies with a focus on data integrity and patient safety, preparing and conducting site visits, and delivering timely monitoring reports.

Clinical Operations at Thermo Fisher Scientific enables global clinical programmes through end‑to‑end trial support. The Clinical Research Associate I monitors sites, ensures protocol compliance, conducts remote and on‑site visits, and manages documentation and data accuracy.

Precision Medicine Group Clinical Research team drives oncology and rare disease trials with a focus on precision medicine. The CRA monitors study progress, coordinates site setup, conducts visits, and ensures compliance with protocol, SOPs, ICH‑GCP and regulatory standards.

Site Management & Monitoring team at AstraZeneca drives clinical studies for innovative cell therapy products. The Clinical Research Associate monitors multi‑site trials (CAR‑T, TCR‑T, Treg), ensures data quality, conducts feasibility, recruitment and closure activities, and collaborates with international study teams.

Fortrea is hiring a Clinical Research Associate I in Germany to transition experienced clinical research professionals into onsite monitoring. You will support clinical trial site management across therapeutic areas such as Oncology, Dermatology, Respiratory, Cardiology, and Diabetes, conducting site initiation, routine monitoring, and close-out visits under CRA mentorship.

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 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.

Clinical Research team at NAMSA conducts global medical device trials ensuring patient safety and regulatory compliance. The Associate monitors sites, conducts qualifications, initiations, interim and close‑out visits, and manages study documentation and metrics.

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.

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 team at Thermo Fisher Scientific conducts risk‑based monitoring of investigator sites to ensure compliance and data integrity for cell therapy trials. The Senior Clinical Research Associate I/II performs on‑site and remote monitoring, data review, and site communication while tracking trial progress and supporting project documentation.

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 Research team at Thermo Fisher Scientific conducts global clinical trials supporting pharma and biotech partners. Senior Clinical Research Associate I, Sponsor-Dedicated FSP monitors investigator sites remotely and on‑site, ensures protocol compliance, performs risk‑based monitoring, data verification, and audit readiness while coordinating with the Clinical Team Manager.

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.

Clinical Research team at Thermo Fisher Scientific supports global pharmaceutical and biotech trials. The Clinical Research Associate II coordinates remote and on‑site monitoring, ensures protocol compliance, conducts risk‑based assessments, and prepares status reports.

Clinical Operations team at Covance supports sponsor‑dedicated clinical trials in Germany. The Unblinded Clinical Research Associate conducts unblinded monitoring, ensures protocol compliance, manages investigational product oversight, and builds site relationships across the Ruhrgebiet and Frankfurt regions.

Clinical Research Associate II at Thermo Fisher Scientific works within the global clinical monitoring team to ensure trial compliance and data integrity across sponsor studies. The role conducts remote and on‑site site visits, performs risk‑based monitoring, documentation review, and collaborates with investigators to resolve findings.

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.

AstraZeneca seeks a Clinical Research Associate for its Site Management & Monitoring team to drive clinical trials in cell therapy. The role involves monitoring studies, ensuring data integrity, and supporting site performance across West Germany.