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Form of workICON 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.
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 requirements
- Participate 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-out
- Perform 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.
You are:
- Bachelors degree or equivalent experience
- Clinical Research and/or understanding clinical trials
- Strong 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:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family's needs
- Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefitsICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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 or submit a request here.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.
Employment Type: OTHER
