Clinical Research Associate Jobs in Germany

Clinical Research Team at Psi CRO focuses on delivering high‑quality clinical trials across therapeutic areas. The CRA conducts onsite and remote monitoring visits, performs CRF review, source verification, and manages site communication while mentoring junior staff.

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.

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.

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.

Allucent’s Clinical Research team drives the monitoring of oncology and rare disease trials, ensuring GCP compliance and data integrity. The Sr. Clinical Research Associate independently manages site initiation, routine monitoring, and close‑out visits across Germany, acting as the primary liaison between sponsors and investigators.

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.

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.

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.

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.

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.

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 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.

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 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.