As a Clinical Research Coordinator you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. This position is located in John's Creek, GA. We are looking for someone with a flexibile schedule and the ability to work weekend hours, if needed!
ResponsibilitiesWhat you will be doing:
Maintain test and control article inventory throughout the study, and perform test and control article reconciliation at study completion.Manage the investigator file (ISF) and other regulatory documents throughout the study by obtaining essential documentation and complying to regulatory and sponsor requirementsParticipate in the SIM, site activation visits (SAV) and interim monitoring visits .Confirm all documents are available prior to study initiation meeting (SIM) and are complete at the study close-outPerform study procedures such as visual acuity, topography, autorefractor commensurate with level of experience/training and as delegated by the PI and documented on the Site Delegation Log.Review and develop familiarity with protocol, study timelines, inclusion and exclusion criteria.Facilitate monitoring visits.Back-up for Clinical Research Scheduling Coordinator.Assure timely completion of Case Report Forms (CRFs) and responds to queries in a timely manner.Work with the PI to manage day to day activities of the study including subject scheduling, problem solving, communication and protocol management.Retain all study records in accordance with sponsor requirements.Work with PI to develop and implement recruitment strategies in accordance with IRB/IEC requirements. QualificationsYou are:
Bachelors degree or equivalent experienceClinical Research and/or understanding clinical trialsStrong communication and collaboration skills
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.