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.

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.

We are looking for a Clinical Research Associate / Senior Clinical Research Associate to join a highly motivated, international team where collaboration, ownership, and trust are part of everyday work. Hybrid role in Munich/Planegg or Home-based in Germany

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.

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.

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.

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.

Parexel's Clinical Operations team in Berlin seeks a driven student to support clinical trial operations and data excellence. As an Associate Clinical Research Nurse, you will admit and orient study participants, perform clinical measurements and sample collection, prepare monitoring equipment, and handle documentation and data entry.

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.

IQVIA's Clinical Site Management department seeks a Clinical Research Associate 1 or 2 to conduct comprehensive clinical trial monitoring across multiple sponsors and indications throughout Germany. Day-to-day, you will perform site selection, initiation, monitoring, and close-out visits; evaluate site quality and integrity against GCP and ICH guidelines; track regulatory submissions, recruitment, CRF completion, and data query resolution; and collaborate with study-site experts and client repre

Flexible Solutions at Fortrea drives innovative oncology drug development in Germany. The CRA manages site selection, monitoring, and close‑out while mentoring new staff and serving as SME in client‑specific projects.

IQVIA’s Clinical Functional Service Partnership team delivers comprehensive clinical trial management for a single pharma client. As a Trainee Clinical Research Associate, you will conduct site selection, initiation, monitoring, and close‑out visits, support recruitment plans, and manage regulatory submissions and data queries.

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.

IQVIA Clinical Research Associate team builds and monitors clinical trials for single‑sponsor clients across therapeutic areas. The role performs site selection, initiation, monitoring, and close‑out visits, supports recruitment plans, and ensures GCP/ICH compliance.

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.