Clinical Trial Manager, Junior

We are hiring a Clinical Trial Manager (junior level to work as Senior Associate Study Manager/SASM) - the role is homebased in teh UK with no travel

This is a great opportunity to steer your career towards clinical trial management. It would suit a Junior CTM or experienced Senior Clinical Project Specialist looking for their first CTM position.

The role

The CTM (SASM) support the Global Clinical Trial Manager (GCTM), Global Early Clinical Development Manager (GECDM), Local Trial Manager (LTM) Regional or Country Study Manager in the delivery of the clinical and operational strategy and assist the execution of clinical trials

What is offered

• Full-time and permanent contract of employment with us seconded to one single sponsor
• The role is NOT open to Freelancers/Freelance Contractors
• The role is homebased in the UK/England
• Salary according to level of skills and experience
• Company benefits and annual leave

Why Join?

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.

What is required

• BS/BA/BSc in the sciences preferred or RN or above
• 5 years’ work experience in life sciences or medically related field, including 2 years of direct biopharmaceutical clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company
• Some oversight experience of outside clinical research vendors (CROs, central labs, imaging vendors, etc.)
• Experience as Senior Project Specialist or Senior CRA can be considered as this is a great career move into clinical trial management
• Working knowledge of international clinical trial management is a plus
• Knowledge of International Conference on Harmonization (ICH), Good Clinical Practice
• (GCP), and applicable international regulations and guidelines, including risk management principles for clinical trials