AstraZeneca UK CRA (Biopharma division)

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.

Are you an experienced Independent Monitor/CRA searching for your next role in an excellent working environment, with opportunities to advance within a growing department? Our Global partner is looking for permanent, established and dynamic home-based CRAs in the UK.

Learn alongside other talented individuals @ ICON and you’ll be working in a large team of experienced and knowledgable (non-Oncology) Clinical Research Associates.

Duration: These are all full-time, permanent positions.

The CRA is responsible for the preparation, initiation, monitoring and closure of an agreed number of centres in Biopharma clinical trials.

Amongst other tasks, your main responsibilities will be to;

• Contribute to the selection of potential investigators.
• Provide the required monitoring visit reports within required timelines
• Drive performance at the sites. Proactively identify study-related issues and escalate as appropriate.
• Perform source data verification according to SDV plan and ensure data query resolution
• Initiate, monitor and close study sites in compliance with client Procedural Documents. Share information on patient recruitment and study site progress within local Study Delivery Team.
• Train, support and advise Investigators and site staff in study related matters.

• What is Required
• Ability to travel regionally as required (you must already be based in the UK and have the right-to-work in the UK).
• Life science university degree (minimum BSc),
• Minimum 2 years' Industry experience in an independent clinical monitoring role.

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.