Research associate Jobs in Ottobrunn
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Research associate • ottobrunn
- Gesponsert
Clinical Research Associate (CRA) - cardivascular area
PharmiwebMunich, DESenior Clinical Research Associate I
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Hydrogen Research Specialist - Germany
Sungrow EuropeMunich, Bavaria, Germany- Gesponsert
Professor in » Solid-State Quantum Systems «
Technische Universität München (TUM)München, DeutschlandResearch Associate (Postdoc) Position (m / f / d) in B Cell Immunology
Klinikum rechts der IsarMünchen, Bayern, DE- Gesponsert
Founders Associate
FUNDEDMunich, Bavaria, GermanyClinical Research Associate II, Dermatology & Rheumatology, Germany
InderoMunich, BY, DE- Gesponsert
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MED-EL Medical ElectronicsInnsbruck (Österreich), Germany- Gesponsert
Research Engineer (m / f / d)
MED-ELMünchen, Bayern, GermanyResearch Associate (Doctoral Student) (m / f / x) in Entrepreneurship and Family Enterprise
Technical University of MunichMunich, DE- Gesponsert
Working Student - Market Research all genders
zooplus SEMunich, Bavaria, Germany- Gesponsert
Sales Associate
Audemars PiguetMunich, Bavaria, GermanySenior Clinical Research Associate - Germany - Home based
Worldwide Clinical TrialsMunich, GermanyResearch Assistants - Munich
Clyde & CoMunichContent Creator : Schwerpunkt Research Reports
Julian HospMunich, Bavaria, Germany- Gesponsert
Working Student - Clinical Research
BrainlabMunich, Bavaria, GermanyFounders Associate
TOC The Onaran Company GmbHMunich, Bavaria, GermanyClinical Research Associate (CRA) - cardivascular area
PharmiwebMunich, 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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