Clinical Research Associate Jobs in Thuringia, 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.

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.

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 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.

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.

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.

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.

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 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.

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.

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.

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.

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.