Clinical Research Associate Jobs in Saxony, Germany

Clinical Research Associate (CRA) (m/w/d) – Onkologie (field‑based) at AstraZeneca. Responsible for monitoring oncology clinical trials across Berlin, Magdeburg, Leipzig, Dresden.

Clinical Research Associate (CRA) – Onkologie – responsible for monitoring oncology clinical trials across Eastern and Southern Germany, ensuring accurate, timely data collection and compliance with ICH‑GCP, AMG and other regulations. Duties include feasibility assessment, site initiation, recruitment, ongoing monitoring, database lock, closure, and reporting.

Global Clinical Monitoring and Site Management at Premier Research drives the delivery of life‑changing medicines by ensuring data integrity and patient safety. The CRA II monitors clinical studies, prepares monitoring reports, and maintains the Trial Master File in accordance with ICH/GCP.

Clinical Research Associate IQVIA Czech Republic is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization. Your responsibilities will include: - Performing site selection, initiation, monitoring and close-out visits - Supporting the development of a subject recruitment plan - Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines - Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions - Collaborating with experts at study sites and with client representatives Qualifications: - University degree in scientific discipline or health care - Experience in Pharma Industry, and/or Clinical Trials environment - Very good computer skills including MS Office - Excellent command of Czech and English language - Organizational, time management and problem-solving skills - Ability to establish and maintain effective working relationships with coworkers, managers, and clients - Flexibility to travel - Driver’s license class B What you can expect: - Resources that promote your career growth - Leaders that support flexible work schedules - Programs to help you build your therapeutic knowledge - Excellent working environment in a stabile, international, reputable company - Mobile phone and attractive benefits package IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

IQVIA CZ Republic seeks a Junior Clinical Research Associate to join Sponsor dedicated team. Responsibilities include site selection, initiation, monitoring, close-out visits, recruitment plan development, quality evaluation per GCP and ICH, regulatory submission tracking, data query resolution, collaboration with site experts and client reps.

Clinical Research Associate II at Thermo Fisher Scientific’s PPD Czech Republic team drives clinical monitoring across 2,700 trials worldwide. The role conducts risk‑based site visits, ensures ICH‑GCP compliance, and manages audit readiness while coordinating with investigators and sponsors.

Clinical Research Associate responsible for planning, implementing, and managing clinical trials for Kerr Dental products in the EU. Develops trial protocols, SOPs, and CRFs, and oversees clinical evaluations and post‑market surveillance (PMS) activities, including customer surveys and systematic literature reviews. Coordinates preparation of Clinical Evaluation Plans (CEPs), Clinical Evaluation Reports (CERs), Post Market Surveillance Plans, and safety summaries in compliance with EU MDR. Works closely with Regulatory teams on document strategies, compiling data into comprehensive regulatory packages.

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.

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 team at Novartis drives clinical trials from site initiation to completion, ensuring high‑quality data and patient safety. The Senior Clinical Research Associate manages site relationships, conducts on‑site and remote monitoring, resolves risks, and collaborates with cross‑functional teams to advance Phase I‑IV studies.

Clinical Research team at ProPharma Group provides regulatory and monitoring expertise for biotech and pharma drug development. The Senior Clinical Research Associate conducts site monitoring, initiates studies, manages documentation, and ensures compliance with GCP and local regulations.

Clinical Services – Clinical Study Delivery team at Alimentiv oversees clinical site monitoring and management for multinational studies. The Senior Clinical Research Associate leads monitoring activities, mentors CRAs, coordinates site recruitment, ensures compliance, and acts as primary liaison with sponsors.

IQVIA seeks a Clinical Research Associate to support a sponsor, performing visits per ICH-GCP, managing patient recruitment, RCA/CAPA, reporting, eTMF, and collaborating with study teams. Requires MSc/BSc in Health Sciences, Czech and English proficiency, 1+ year CRA experience, CTMS/eTMF/EDC knowledge, travel availability, and driving license.

Parexel FSP is expanding its oncology clinical research team to support a key sponsor. The Senior Clinical Research Associate will manage site activation, monitoring, and close‑out for clinical trials, ensure compliance with GCP and local regulations, and coordinate safety reporting and audit activities.