Clinical Research Associate Jobs in North Rhine-Westphalia, Germany

Clinical Research team at IQVIA focuses on delivering high‑quality clinical trial support for single‑sponsor studies. The role conducts site selection, initiation, monitoring and close‑out visits, manages regulatory submissions and recruitment tracking, and mentors junior staff while collaborating with site experts and client representatives.

Seeking experienced Clinical Research Associates to manage multi-site studies in the Netherlands, focusing on medical devices. Candidates will oversee site performance, conduct monitoring visits, and ensure high-quality deliverables while collaborating with sponsors and internal teams.

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.

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.

AbbVie is seeking a Clinical Research Associate I to join its Research and Development team in Wiesbaden, Germany, within the Clinical Site Management department. In this role, you will be responsible for implementing global clinical trials in Germany, managing study selection, conduct, and close-out, coordinating with local CRA colleagues, monitoring investigational sites, and ensuring compliance with internal and external regulations.

Precision Medicine Group Clinical Research Team advances oncology and rare disease trials by integrating cutting‑edge data science with trial execution. The Clinical Research Associate II monitors study progress, conducts site visits, and ensures compliance with protocols, 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.

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.

Clinical Monitoring Team at Thermo Fisher Scientific conducts site oversight for global clinical trials. The Senior Clinical Research Associate I performs remote and on‑site monitoring, ensures protocol and ICH‑GCP compliance, and manages documentation and risk‑based monitoring activities.

WEP Clinical drives end-to-end clinical trial delivery to accelerate patient access to new therapies. The Senior Clinical Research Associate oversees on-site and remote monitoring, ensures protocol compliance, and mentors junior CRAs across multiple studies.

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.

AbbVie's Research and Development team in Wiesbaden, Germany, is hiring a Clinical Research Associate I to support clinical trials for innovative medicines. In this role, you will manage a selection of studies from site selection through completion, coordinate with local CRA colleagues, monitor investigational sites, and ensure compliance with internal and external regulations.

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.

Senior Clinical Research Associate responsible for full clinical site monitoring services across multiple multinational projects in Belgium. In-house role overseeing design and oversight of monitoring services, including training, site recruitment, data/document management, budget monitoring, and regulatory filings aligned with SOPs, GCP, and study guidelines.

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 Operations team at Bristol Myers Squibb ensures high‑quality, compliant clinical trials across Germany. The Clinical Research Associate monitors site qualification, initiation, routine visits and close‑out, verifies data integrity, and supports investigators while adhering to ICH GCP and SOPs.