Clinical Research Associate Jobs in Baden-Wurttemberg, 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.

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.

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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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.

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.

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.

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.

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.

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.

Clinical Research team in the Department of Circulation, Thorax, Transplant at University Hospital Basel conducts clinical studies focusing on patient monitoring and project coordination. The role supports study setup, monitoring visits, data management, and ensures regulatory compliance.

The Country Clinical Research Lead (CRL) role within IQVIA’s sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department supports a key client’s project team in executing clinical trials across multiple therapeutic areas. Day-to-day, the CRL oversees local CRO activities, serves as the single point of contact for strategic outsourced studies, conducts top-level feasibilities, partners with study startup specialists and CRAs on regulatory submissions, and acts as a site r

Thermo Fisher Scientific invites pharmacy students to launch their careers through a 6‑month Clinical Operations internship. The role offers hands‑on exposure to global clinical trials, administrative support, and cross‑functional collaboration across Europe.

The Site Manager (SM) is engaged in facilitating the conduct of clinical studies. Specific focus is put on patient related site support, with the aim to maximise the utilisation of site staff designated to a given study (e.g. study site coordinator, study nurse, sub-investigator) through provision of site training and oversight for logistically / technically more demanding study procedures.

The Site Manager (SM) is engaged in facilitating the conduct of clinical studies. Specific focus is put on patient related site support, with the aim to maximise the utilisation of site staff designated to a given study (e.g. study site coordinator, study nurse, sub-investigator) through provision of site training and oversight for logistically / technically more demanding study procedures.

Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMP in Frankfurt am Main seeks a Biostatistician in Clinical Research to support clinical development and scientific evidence generation. Day-to-day work includes statistical planning and methodological development of clinical studies and research projects, statistical consulting, creation and review of study documents (protocols, SAPs, TFLs, reports), reproducible analysis of study data, and collaboration with clinical project ma

IT Law & Interdisciplinary Privacy Research department at Fraunhofer SIT and the ATHENE office conduct cutting‑edge research on data protection and cybersecurity law while providing legal and contractual support for the institute. The Research Associate splits time between scholarly work—writing articles on German and US law, analyzing privacy regulations—and operational duties such as drafting, reviewing and negotiating national and international contracts.

Testlab Mobile Security department at Fraunhofer SIT conducts cutting‑edge research in cybersecurity. The Research Associate performs deep static software analysis of native iOS apps, detecting errors and evaluating software quality while adapting analysis approaches to new platforms.