Clinical Trial Assistant Brentwood TN
About the role
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"At ICON, it's our People that set us Apart"
Are you interested in improving your knowledge of Clinical Trials and contributing to our culture of process improvement with a focus on streamlining our processes of adding value to our business and meeting client needs?
Clinical Trial Assistant role within ICON:
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. As a Clinical Trial Assistant (CTA) you have to assist the clinical research teams in ensuring the most effective and efficient conduct of clinical research studies by providing administration and project tracking support.
The successful candidate will show capability in the areas of general administrative support to the Clinical Operations Department and assistance to Project Managers and Project Directors, assist the Clinical Operations teams in completion of all required tasks to meet departmental and project goals, support the Clinical Operations teams with ongoing conduct of studies. Familiar with ICH GCP, appropriate regulations.
We are presently in over 40 countries with over 80 offices worldwide and over 10K employees globally. We are comprised of 6 divisions and offer a full-service portfolio of solutions to our clients.
Benefits of working at ICON:
We provide a Study Start Up Associate with the resources to be successful and visibility by having them provide input and recommendation to upper management on the study start up submission process and how to better the work process. In addition, we offer excellent health, dental, vision and life insurance coverage; 401(K) with company match; competitive pay; generous time off; and bonus incentives
Minimal travel may be required (10%)
To succeed you will need:
A Bachelor’s Degree preferably in life sciences will ensure your familiarity with regulatory guidelines and industry knowledge. Minimum of 1 year of experience preparing, reviewing and submitting submissions to ethics, regulatory, and other relevant authorities in order to obtain all necessary authorizations/approvals pertaining to clinical trial conduct
We invite you to review our opportunities at www.iconplc.com/careers.
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
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