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Clinical Trial Assistant

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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.
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