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Clinical research associate Jobs in Düsseldorf
- Gesponsert
Clinical Research Associate (CRA / SCRA) - sponsor dedicated
PharmiwebDüsseldorf, DEEnglish into French Medical Translators (Clinical Research documents) Remote
WelocalizeDusseldorf, Germany(Senior) Research Manager (w / m / d)
Enterprise IT Experts - Rüdiger MohneDüsseldorf, Nordrhein-Westfalen, DEWerkstudent Koordination Data Research (w / m / d)
Versatel GmbHDüsseldorfAssociate Intern
McKinsey & CompanyDusseldorfClinical Trial Associate (m / w / d)
HaysMonheim- Gesponsert
Postdoc - Ion Channel Research (m / f / d)
Universitätsklinikum Aachen AöRGrevenbroich, Nordrhein-Westfalen, GermanyAssociate - Consulting
Vivaldi GroupDüsseldorf, NRW, DESr Tech Lead Manager - Applied Research
0333 eBay Group Services GmbHDusseldorfSenior Associate (2025 PhD / ABD graduates) (Competition practice)
Charles River AssociatesDusseldorf, GermanyResearch Manager (mensch)
annalectDüsseldorf, Nordrhein-Westfalen, DeutschlandClinical Sales Associate
IntuitiveDuesseldorf, DE- Gesponsert
Praktikanten (m / w / d) Economic Research Germany
HSBC Continental Europe S.A., GermanyDüsseldorfCategory Associate
PicnicDüsseldorf, North Rhine-Westphalia, GermanyAssociate
Jones DayDusseldorfResearch Consultant (m / w / d)
hrXpertsDüsseldorf, DeutschlandClinical Sales Associate
Intuitive SurgicalDuesseldorf, Germany(Senior) Manager, Medical Science Liaison, Therapy Development, Transcatheter Mitral and Tricuspid Therapies (Germany)
Edwards LifesciencesGermany, Nordrein Westfalen, RemoteMarket Research Manager, LIXIL Europe (d / f / m)
Grohe AGDüsseldorf, Nordrhein-Westfalen, DeutschlandClinical Research Associate (CRA / SCRA) - sponsor dedicated
PharmiwebDüsseldorf, DEICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Clinical Research Associate II at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP.
You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people´s lives. Working in this program you will feel challenged and supported to advance in your professional career while making a truly impact.
What you will be doing :
- Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
- Submitting protocol, consent documents for ethics / IRB approval, as well as preparing regulatory submissions
- Balancing sponsor generated queries
- Taking responsibility for study cost efficiency
- Preparation and review of study documentation and feasibility studies for new proposals
- Potential to assist in training and mentoring fellow CRAs
You are :
What ICON can offer you :
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include :
Visit our careers website to read more about the benefits of working at ICON : https : / / careers.iconplc.com / benefits
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
https : / / careers.iconplc.com / reasonable-accommodations
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
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