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Clinical research Jobs in Richmond, VA
Clinical Research Associate
PRA Health SciencesVA, US- Promoted
Research Nurse
JouléRichmond, VA, United States- Promoted
Research Assistant (Remote)
D Aceto Services LLCRichmond, VirginiaClinical Research Coordinator / Clinical Research Coordinator, Licensed
Commonwealth of VirginiaRichmondCLINICAL RESEARCH COORDINATOR, CARDIOVASCULAR (FT / Days)
Centra HealthVA, United States- Promoted
- New!
Research Compliance Specialist
The Ohio State UniversityRichmond, VA, United StatesResearch Nurse
JobsRUs.comRichmond, VA, United States- Promoted
Market Research Analyst
ISC2Richmond, VA, United StatesResearch Recruiter
CoStar GroupVA Richmond, US- Promoted
- New!
Senior Operations Research Analyst
The MITRE CorporationDhs, VA, USResearch Scientist
bemcontrolsVirginia, United StatesResearch Engineer
Carpenter Co.Richmond, VA- Promoted
Director, Research Account Management
Royall & CompanyRichmond, VA- Promoted
Research Assistant Intern
iQuasar LLCUniversity of Richmond, VA, United StatesResearch Analyst
WelocalizeVirginiaClinical Research Coordinator / Clinical Research Coordinator, Licensed
Virginia Commonwealth UniversityRichmond, VA, USResearch Assistant
Nomad Chronicles, Virginia, ,- Promoted
Research Nurse : 364366
JobsRUsRichmond, VA, USResearch Analyst
London Company of VirginiaRichmond, VA, USA- Promoted
Clinical Research Nurse Practitioner
SQRLRichmond, VA, USClinical 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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