CTA
About the role
This vacancy has now expired. Please click here to view live vacancies.
"At ICON, it's our People that set us
Apart"
Do you
have experience assisting clinical research teams to ensure effective and
efficient conduct of clinical research studies by providing administration and
project tracking support?
CTA
role within ICON:
ICON
has a strong reputation in our approaches to clinical development. We apply scientific and operational
excellence across all phases of clinical trial outsourcing services for our
clients. We work with top
pharmaceutical organizations on emerging therapeutic areas which include but
are not limited to Oncology, Vaccines, CNS, Cardiovascular and Pain. We are presently in over 40 countries with
over 80 offices worldwide and over 10K employees globally.
The
CTA will provide general administrative support to the CRA’s and assistance to
project managers/directors to ensure completion of all required tasks and
studies. You will set up, organize and
maintain clinical study documentation (e.g. Main Study Files, CRFs, etc.) including
preparation for internal/external audits, final reconciliation and archival.
You will process
Data Collection Forms (i.e. log in, tracking, quality control as appropriate
for the study) and assist in quality control audits of clinical study
documentation (e.g. Main Study Files, CRF Files, Monitoring Files, etc.). You will be responsible for co-ordinate
ordering/dispatch and tracking of trial materials (e.g. CRFs, diary cards, lab
supplies, drug supplies) as appropriate.
Benefits
of working at ICON:
In addition
to partnering with the top pharmaceutical and biotech companies in the world we
offer a strong benefits package that includes a comprehensive health plan,
retirement plans, competitive pay, bonus plans, vacation, and other incentives.
To
succeed you will need:
We are
seeking candidates with a Bachelor’s Degree or location equivalent or High
School Diploma with research or health care related academic or work experience
preferable.
To be
successful you will need to be familiar with ICH, GCP appropriate regulations
and to have good organizational skills and the ability to manage multiple tasks
and meticulous attention to detail, good written and verbal (spoken English)
communication skills and have experience with Microsoft Word, Excel, PowerPoint,
Outlook.
We
invite you to review our opportunities at www.iconplc.com/careers.
What’s Next?
Following your application you will be contacted by one
of our dedicated recruiters and if successful we will be able to provide you
with more details about this opportunity.
ICON is an equal
opportunity employer - Minorities/Females/Disabled/Veterans and committed to
providing a workplace free of any discrimination or harassment.
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. See all locations Learn more about Our Culture at ICON
Day in the life
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Teaser label
IndustryContent type
BlogsPublish date
07/07/2025
Summary
Precision at the Outset: The Strategic Role of Site Selection and Activation in Clinical Trials The success of any clinical trial begins well before the first patient is enrolled. Behind every sit
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Teaser label
IndustryContent type
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07/04/2025
Summary
Cybersecurity in Clinical Data Management In clinical research, data is both a vital asset and a significant responsibility. As trials become increasingly digitised and decentralised, the protectio
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Teaser label
IndustryContent type
BlogsPublish date
07/03/2025
Summary
Finding the Specialisation for You Clinical research is a dynamic, multidisciplinary field that brings together scientific innovation, operational rigour and patient-centric thinking. While many
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