Clinical Research Associate Jobs in Rheinland-Pfalz, Germany

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.

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.

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 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 TFS HealthScience drives the execution of Phase II and III oncology trials across Europe. The Clinical Research Associate independently plans, conducts, and follows up on site initiation, monitoring, and close‑out visits, reviews eCRF data, ensures regulatory compliance, and collaborates with medical, project management, quality, and data teams.

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.

IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. As a Clinical Research Associate 2, you will perform site selection, initiation, monitoring and close‑out visits, support recruitment plans, evaluate site practices against GCP and ICH, track regulatory submissions and data queries, and mentor junior team members.

Join IQVIA as a Clinical Research Associate II to support clinical trials across Germany and Switzerland. You will conduct site selection, initiation, monitoring, and close‑out visits, develop recruitment plans, ensure GCP compliance, and manage regulatory submissions.

BeiGene’s Clinical Research Associate team drives oncology and hematology trials across Germany, ensuring compliance with ICH and GCP. The role monitors sites, manages recruitment, resolves data queries, and collaborates with the Regional Clinical Operations Manager to meet study milestones. Working remotely, the associate supports site feasibility, training, and inspection readiness while traveling up to 60% for site visits.

Cardiac Management Solutions division of ZOLL Medical develops life‑saving cardiac devices such as the LifeVest wearable defibrillator. The Clinical Research Associate supports EMEA clinical trials, managing site monitoring, regulatory documentation, and cross‑functional coordination to ensure protocol compliance and data quality.

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 Associate (CRA) (m/w/d) – Region Mitteldeutschland/Raum Frankfurt at AstraZeneca. The role is field‑based and permanent, focusing on monitoring clinical trials across immunology, respiratory, metabolic and cardiovascular indications.

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.