Clinical Research Associate Jobs in City state Bremen, Germany

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.

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.

Linical seeks a Clinical Research Associate II in Germany to manage the feasibility, initiation, monitoring, and close-out of investigative sites. The role ensures participant safety, regulatory compliance with GCPs, and data integrity through source verification and site oversight.

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.

TFS HealthScience’s Ophthalmology team seeks a Freelance Senior Clinical Research Associate to support clinical development projects. The role involves initiating, monitoring, and closing out study sites both on-site and remotely while ensuring regulatory compliance and data integrity.

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 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 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 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 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.

As part of our CDS Oncology and Dermatology teams you will be working alongside passionate and innovative professionals to ensure our customers achieve their goals. The Clinical Research Associate will function operationally as a member of a Project Team and is responsible for the initiation, on–site and/or remote monitoring, close out of study sites during study conduct, according to company policies, SOPs and GCP and ICH guidelines and other regulatory requirements.

This role will be responsible for site monitoring activities to ensure the overall integrity of study implementation and adherence to study protocol at assigned clinical sites. This role will be to work on medical device trials in Cardiology.

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.

Make a meaningful impact in clinical research by joining our sponsor-dedicated team as a Clinical Research Associate (CRA) . This role offers the opportunity to monitor sites in Austria and in Switzerland , while working on cutting-edge studies that shape the future of healthcare.

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.

As the Clinical Research Director, you will spearhead cutting‑edge ophthalmic studies, guiding product development through trials, ensuring safety, efficacy, and regulatory compliance to advance eye care.

BeOne Medicines Germany GmbH leads clinical research initiatives to develop innovative cancer therapies. The Clinical Research Manager oversees trial monitoring staff, drives study start‑up, ensures GCP compliance, and partners with regional operations to meet timelines and quality standards.

IQVIA Clinical Research team coordinates a multi‑site clinical study in Erfurt, ensuring patient safety, data integrity, and protocol compliance. The coordinator manages study visits, EDC data entry, query resolution, and collaborates with investigators and monitors.

Wissenschaftlicher Mitarbeiter (Research Associate) im Bereich akademische Beratung in Bonn, Nordrhein-Westfalen, Deutschland. The role supports medical doctoral candidates through the entire scientific process—from topic development to completed dissertation—by providing methodological, content, and scientific guidance.