product and service quality. Support sponsor responsibilities in clinicaltrials , ensuring adherence to regulatory... Management Systems (QMS) and process development in complex environments (e.g., clinicaltrials) Knowledge of quality standards...
in clinicaltrials, ensuring adherence to regulatory and ethical standards. Plan and conduct internal and external audits... environments (e.g., clinicaltrials) Knowledge of quality standards and regulatory requirements (e.g., ICH GCP, EU GMP...
while gaining direct experience with one of our clients. Furthermore you will gain experience covering clinicaltrials in Germany...Join IQVIA as a Clinical Research Associate 2 / CRA II and work home-based in Southern Germany or in the Frankfurt area...
, and format a wide range of documents (of low to high complexity) required for research, non-clinical, clinical development... in BioNTech-relevant indications. drafting alone new or updated CTPs and CSRs required for Phase I-III trials. drafting low...
The IQVIA Sponsor-Dedicated ClinicalTrials Assistant Team is supporting the project teams in the execution of clinical... trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research...
as a Clinical Research Associate 2 / CRA 2 (m/w/d) in home-office throughout Germany and help shape the future of patient care... intersection of clinical research and technology, this is the perfect opportunity to make a lasting impact. Your responsibilities...
sites (test centres and hospitals) worldwide. Even if you don't have any experience in the world of clinicaltrials... to strengthen our international Clario team! Be a part of driving clinicaltrials faster with your daily performance...
, with opportunities to influence critical processes and contribute to groundbreaking advancements in clinicaltrials. Join us in shaping...Mainz, Germany | full time | Job ID: 10688 About the Role: As Director, Process Improvement for Global Clinical...
) at our Estenfeld (near Würzburg) site to strengthen our international Clario team! Be a part of driving clinicaltrials faster... world of clinicaltrials, we are happy to show you! What We Offer Flexible working hours and working time accounts...
of investigational medicinal products (IMPs) and associated materials to patients participating in our clinicaltrials. You will manage..., and DS-DP transfers and imports worldwide. Serve as point of contact for clinical-site shipment queries and troubleshooting...