CTA Cambridge UK

As a CTA, you will be dedicated to an innovative and global Biotechnology company, who pride themselves to be one of the world's leading independent biotechnology companies. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society today.

What you will be doing:

• Study start-up activities, including creating site folders, collating, preparing and maintaining (e) SIP documents, updating systems
• Liaising with clinical sites to collect, review and track feasibility questionnaires
• Coordinating and maintaining local data into study management systems including setting up new studies in eClinical
• Organise and participate in Investigator meetings and monitor workshops as required within budget guidelines
• Orders, processes and tracks Case Report Forms (CRF) and follows up on query resolution if required to do so
• Interacts with Clinical Research Services Manager for project or study related work
• Supports the execution of clinical studies
• Responsible for study start up activities
• Tracks study related documents
• Promotes operational and scientific excellence
• Identifies opportunities and best practices with local and regional partners that will contribute to overall operational effectiveness

What is offered

• Hybrid position: office-based in the Cambridge office with 1 day homeworking days
• Full-time
• Salary will be offered depending on level of experience and skills
• Permanent contract of employment with company perks and benefits

You are:

• Holder of a Bachelor’s degree ideally within health sciences or qualified nurse
• A clinical trial coordinator or administrator with a passion for clinical research
• Able to work efficiently and accurately with MS Office and EDC systems
• Able to work with different electronic systems to coordinate clinical trials with excellent and accurate attention to detail when entering data onto systems/database
• Holding a valid, current UK working eligibility

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.