Clinical Research Associate Jobs in Saxony, Germany

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.

The Clinical Research Associate 2 at AbbVie advances the company's clinical research pipeline by ensuring proper trial conduct, data integrity, compliance, and customer experience across immunology, oncology, neuroscience, and Allergan Aesthetics. Day-to-day, the role serves as the primary site contact, conducts site evaluation, routine, and closure monitoring, trains and motivates site staff and principal investigators, performs risk-based monitoring, mentors junior CRAs, and ensures audit and

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 - Supp

TFS HealthScience’s Ophthalmology team within Clinical Development Services seeks a Freelance Senior Clinical Research Associate to support anticipated clinical trials. The role involves initiating, monitoring, and closing out study sites both on-site and remotely while ensuring regulatory compliance and data integrity.

Parexel's Clinical Operations team in Berlin seeks a driven student to support clinical trial operations and data excellence. As an Associate Clinical Research Nurse, you will admit and orient study participants, perform clinical measurements and sample collection, prepare monitoring equipment, and handle documentation and data entry.

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.

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.

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators.

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.

Clinical Research Nurse at Thermo Fisher Scientific in Prague oversees multiple clinical trials, ensuring compliance with FDA/GCP and ICH guidelines. The role involves recruiting, enrolling, and retaining participants, performing study procedures such as informed consent, vital signs, ECGs, and blood sampling, and maintaining accurate documentation on case report forms.

Clinical Research Nurse at Parexel supports clinical trials in Berlin, ensuring patient safety and accurate data collection. The role coordinates study activities, manages CRFs, and collaborates with monitors and sponsors.

Clinical Research Nurse at Thermo Fisher Scientific responsible for managing multiple concurrent clinical studies in Prague. Executes study procedures per GCP/ICH, ensures accurate documentation, and maintains data quality and participant safety.

Thermo Fisher Scientific’s Clinical Research Nurse team in Prague conducts clinical studies under Czech legislation and ICH guidelines. The role involves patient care, vital sign monitoring, ECGs, pregnancy tests, and data entry into sponsor systems, ensuring protocol compliance and patient safety.

Clinical Research team at Synaptikon GmbH, the leading company for digital neuropsychological solutions. Designs and evaluates clinical investigation protocols, creates statistical analysis plans, and integrates findings into digital therapies while collaborating with global clinicians and scientists.

Boston Scientific Clinical Engineering team advances innovative cardiac technologies. The Senior Field Clinical Engineer executes day-to-day clinical trial activities across Czechia and Europe, providing technical support in EP procedures and acting as the primary liaison for investigators.

Boston Scientific Clinical Engineering team advances cardiac technologies by supporting pre- and post-market trials across Europe. The Senior Field Clinical Research Engineer executes day-to-day trial activities, serves as primary technical liaison for investigators, provides hands‑on EP support, and leads site qualification and enrollment readiness.

We are currently recruiting a Clinical Research Physician to join our Early Phase Clinical Unit (EPCU) in Berlin. In this role you would act as co-investigator on phase I and II studies, ensure the safety of their trial participants at all times and support the Principal Investigator in preparation, organization, conduct and report of clinical trials according to protocol, Standard Operating Procedures (SOPs), ICH-GCP and local regulations.

Legal Team at Via supports the mission to transform public transportation with smart, data-driven networks. The associate reviews contracts, conducts regulatory research, tracks GDPR compliance, and improves legal processes using internal data systems.