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Clinical research manager Jobs in Chesapeake, VA
Clinical Research Associate
PRA Health SciencesVA, USClinical Research Coordinator - Non RN
Eastern Virginia Medical SchoolNorfolk, VA, US- Promoted
Clinical Research Coordinator
Virginia Oncology AssociatesNorfolk, VA, United StatesClinical Research Coordinator
Odyssey SystemsPortsmouth, VA, US- Promoted
CLINICAL NURSE, CLINICAL PROGRAM MANAGER
CICONIX, LLCVA, United StatesCLINICAL RESEARCH COORDINATOR, CARDIOVASCULAR (FT / Days)
Centra HealthVA, United StatesManager, Clinical Operations
SentaraSentara Park 1300Senior UX Research Operations Manager
ALTERYXVirginia, USA, Remote- Promoted
Clinical Manager
ChenMedNorfolk, VA, USClinical Research Assistant
ActalentPortsmouth, Virginia, USA- New!
RN CLINICAL MANAGER HOSPICE
AmedisysVA, United States- Promoted
Dialysis Clinical Manager Registered Nurse, RN
Fresenius Medical CarePortsmouth, VA, United StatesClinical Research Associate
Childrens Hospital of The King's DaughtersNorfolk, Virginia, United States, 23502Research Manager
Insight TherapeuticsNorfolk, VA- Promoted
Metals Research Engineer
Genex SystemsDhs, VA, USClinical Manager
amedisysChesapeake, Virginia- Promoted
- New!
Clinical Research Coordinator
Eximia ResearchNorfolk, VA, United States- Promoted
Research Analyst / Evaluator
Destinationone ConsultingNorfolk, VA, United StatesClinical Research Associate
PRA Health SciencesVA, 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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