Clinical Research Associate Jobs in Hesse, 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 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.

IQVIA Clinical Research team conducts clinical monitoring visits to ensure study integrity and regulatory compliance. The Clinical Research Associate performs site monitoring, protocol training, quality oversight, progress tracking, and documentation while collaborating with study 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.

IQVIA Clinical Functional Services Partnerships (FSP) team focuses on delivering high‑quality clinical research for a single sponsor, acting as the sponsor’s dedicated partner. The Experienced Clinical Research Associate manages site monitoring across France, drives recruitment plans, trains sites, and mentors junior staff while maintaining risk‑based monitoring practices.

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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.

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

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.

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.

Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between the sponsor/Alimentiv and investigative sites by playing a critical role in the execution of clinical study plans.

IQVIA Clinical Functional Services Partnerships (FSP) business is unique. Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our customers.