Clinical Trial Coordinator
- Ireland
- Clinical Monitoring
- ICON Strategic Solutions (FSP)
- Office Based
TA Business Partner
- Icon Strategic Solutions
About the role
This vacancy has now expired. Please click here to view live vacancies.
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
Job Responsibilities:
- Regulatory & Ethics documents
- Essential document collection
- Maintain the TMF/Country/Site Level
- Build & maintain the ISF
- Tracking & distribution of localised ICF at the site level
- Distribute EC/RA packages to sites
- Site Selection
- Clinical Trial Agreement / Set up
- Distribute Welcome Packs to site post QC review
- Track & initiate payment requests with payment teams
- Clinical Monitoring
- Coordinate site staff vendor access
- Track and follow-up on temperature excursions/deviations in a timely man
- Follow-up/escalate vendor issues (wrong/missing/faulty equipment, re-ordering of supplies, DCFs)
- Updates to ISF/ITF
- Print and track distribution of trial-related docs/acknowledgements of specific docs and materials (safety, CTP, IB, newsletters)
- MISC
- Maintaining Veeva CTMS - site/staff information per welcome pack, payment information, other updates related to CTC tasks
Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, 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, 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.
Explore more about ICON
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
A Day In The LifeContent type
BlogsPublish date
04/05/2023
Summary
Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfil
by
Suzaita Hipolito
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