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Clinical research Jobs in Hoffman estates il
- Promoted
Senior Clinical Research Associate - Midwest
KellyElk Grove Village, IL, US- Promoted
Clinical Trials Research Coverage Analyst
Beacon HillIL, United StatesSenior Clinical Research Associate - CNS - Midwest
Worldwide Clinical TrialsIllinois, USA- Promoted
Caregiver Careers : Ascension Borgess HospitalN Neurosciences Institute Clinical Research is hiring!
AscensionElk Grove Village, IL, US- Promoted
Clinical Research Assistant
Mérieux NutriSciencesAddison, IL, USSenior Clinical Research Associate - Central / Midwest
BeiGeneUS, IL, Home- Promoted
Clinical Supervisor
Prime HealthcareElgin, IL, United States- Promoted
- Promoted
Clinical Research Specialist
VirtualVocationsElgin, Illinois, United States- Promoted
Tax Research Specialist
Service Corporation InternationalBuffalo Grove, IL- Promoted
- New!
Clinical Logistics Associate
Firma Clinical ResearchElk Grove Village, IL, US- Promoted
Clinical Psychologist
Neuro Health Arlington HeightsPalatine, IL, United States- Promoted
Academic / Faculty / Research Physician
MM Recruitment GroupNot Specified, IL, United States- Promoted
Clinical Applications Specialist
Alma Lasers60089, IL, USSenior Research Statistician
Highmark HealthIL, Working at Home, Illinois- Promoted
Research Analyst【CMIC, Inc.】
CMIC IncHoffman Estates, Illinois, United StatesClinical Research Associate
PRA Health SciencesIL, USOverview
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Responsibilities
What you will be doing :
Study Planning
- Contribute to the identification of new sites for clinical trials; analyse capability and support CRMA and CSM in making recommendation for trial inclusion.
- Assume ambassadorial role to facilitate communication between sites and Novartis CPO to increase value proposition to investigators.
- Facilitate the preparation and collection of site and country level documents during all phases of the trial. Supports the CSM in the oversight of Country and Site Trial Master Files (TMF). During all phases of the trial ensure archiving per relevant SOP.
- Negotiate investigator remuneration; prepare financial contracts between investigational sites and investigators. Ensure adherence to payment schedule.
Study Execution
Study Close-out
General
Qualifications
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 :
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.
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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