Ref #: 31761

Employment type: Permanent - Full-Time

Location: Cambridge

Posted: 16-Sep-2021

Description

As a CTA you will assist Managers in fulfilling its site management activities and obligations in relation to clinical studies as the primary sponsor of those studies.

You will provide vital support to all study related activities: study start-up activities, including creating site folders, collating, preparing and maintaining documents, updating systems, supporting close out activities

You will ensure collection, review, track and provision of appropriate clinical documents to support regulatory submission and to perform IRB/IEC submissions including when appropriate preparation and submission of all documents to the central and/or local committee

You will organise and participate in Investigator meetings and monitor workshops as required within budget guidelines

You will provide administrative support such as word processing, photocopying, faxing, filing, managing correspondence, presentations preparation, basic computer software support

What is required:
* BA/BS/BSc in the life sciences or RN
* Clinical trial administration and coordination experience
*Work experience in life sciences or medically related field, including biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
* Work involving data entry into systems/databases and/or business support role

What is offered

• Full-time career opportunity
• Scope for career progression
• Excellent structured training for all new starters
• Salary will be offered depending on level of experience and skills
• Permanent contract of employment with company perks and benefits
• Company benefits to include 23 days annual leave plus UK bank holidays, pension, medical health insurance, etc.
• Office-based in Cambridge (UK) - some homeworking flexibility could be offered after the training period

For full job details and to apply, please email e today at Elisabeth.Knighton@docsglobal.com


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.
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, 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.


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