Clinical Research Associate Jobs in Grand Est, France

BeOne Medicines I GmbH’s Clinical Research Associate team drives oncology and onco‑hematology trials, ensuring GCP compliance and site performance. The role monitors sites, manages data quality, and collaborates with regional study teams to meet milestones.

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.

BeOne Medicines I GmbH’s Clinical Research Associate team drives oncology trial excellence by monitoring sites, ensuring GCP compliance, and managing data quality. The role conducts site selection, initiation, routine and closeout visits, documents findings, and collaborates with regional study managers to meet milestones.

Clinical Research Associate (CRA) (m/w/d) – Zelltherapie (Außendienst) at AstraZeneca is part of the Site Management & Monitoring team, driving the monitoring of cell therapy trials such as CAR‑T, TCR‑T and Treg. The role involves on‑site monitoring visits, data quality oversight, and collaboration with international study teams to ensure timely, compliant study conduct.

AstraZeneca’s Site Management & Monitoring team drives clinical trials for cutting‑edge cell therapies such as CAR‑T, TCR‑T and Treg. The CRA monitors study sites, ensures timely data capture, and collaborates with investigators across Germany.

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.

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.

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.

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 team at IQVIA France drives oncology clinical trials by conducting site monitoring visits, administering protocol training, and ensuring GCP compliance. The role manages study progress, maintains TMF/ISF, generates visit reports, and collaborates with cross-functional teams to resolve data queries.

Clinical Research Associate at IQVIA’s France RDS team, responsible for monitoring oncology clinical trials across multiple sponsors. Day‑to‑day duties include site visits, training delivery, compliance oversight, and data query resolution to ensure protocol integrity.

ProPharma seeks a Serbian-speaking Clinical Research Associate for an 18‑month fixed‑term contract. Responsible for monitoring clinical sites in person and remotely, conducting study start‑ups, developing monitoring documentation, reviewing source documents and case reports, managing investigational supplies, monitoring enrollment and adverse events, reviewing regulatory documents, communicating with site personnel and cross‑functional teams, and participating in project meetings.

Merck’s Animal Health R&D team in Schwabenheim seeks a Clinical Research Associate to conduct and monitor veterinary clinical studies, manage logistics, and ensure compliance with GCP and GMP. The role involves protocol training, data entry oversight, and collaboration with sites across Germany and Europe. Hybrid work model with on-site presence in Schwabenheim and up to 30% travel.

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.

Stryker Clinical Research team drives global clinical studies, ensuring quality and compliance across diverse therapeutic areas. As Lead CRA, you pilot site monitoring, mentor junior CRAs, and coordinate multi‑site operations, impacting study success worldwide.

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.

IQVIA’s Clinical Research team in Illkirch‑Graffenstaden and Paris drives global drug development by ensuring sites execute trials per GCP and ICH standards. The role monitors site visits, manages recruitment plans, and maintains Trial Master Files to guarantee data integrity.

IQVIA Clinical Functional Services Partnerships (FSP) team builds quality delivery for a single sponsor, focusing on oncology, neurology, immunology and diabetes studies. The CRA manages 15 sites across France, drives recruitment, conducts monitoring visits 6‑9 days/month, and mentors junior staff.

IQVIA’s Clinical Research team in France ensures study sites comply with GCP and ICH guidelines. The role conducts site monitoring visits, drives recruitment plans, administers protocol training, and maintains Trial Master File documentation.

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.