CTA - relevant experience required

ICON Strategic Solutions; United Kingdom; On-site; GBP 25,000 - 35,000; Full time

Job summary

Join a leading global clinical research organization as a Clinical Support Associate in Central London. Advance your career by supporting project management in clinical trials and contributing to vital healthcare solutions. Enjoy a competitive salary and benefits focused on well-being and work-life balance while making a real impact.

Benefits

Health Insurance

Retirement Planning

Employee Assistance Programme

Flexible Benefits

Various Annual Leave Entitlements

Qualifications

• At least 6 months' experience in a similar role.
• Fluent in English and proficient in Microsoft Office.
• Interest in the pharmaceutical industry and clinical research.

Responsibilities

• Assist Project Managers in clinical studies and support CRA teams.
• Track site budget and process invoices.
• Maintain and update the Trial Master File.

Skills

Organizational Skills

Communication

Proficiency in Microsoft Office

Problem Solving

Education

Degree in Life Science

Job description

Title: Clinical Support Associate
Location: Central London (2 days in the office per week)
Sponsor dedicated

As a CTA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

The CTA plays a fundamental role in the successful execution of global clinical trials by supporting the Local Study Team in the coordination of logistical and administrative tasks at a local level. Our team help to speed the development of life-changing therapeutics and to make a distinctive contribution to the health and well-being of patients.

Key responsibilities in this role include:

• Proactively assisting Project Managers in running of clinical studies and supporting field based CRA teams to maximise study performance and to ensure good quality output
• Working closely with In-House Set Up Team and Project Manages to improve rapid study start up and reduce study start up timelines
• Central point of contact for study related issues across medical and other departments within UK
• Maintaining and updating of the Trial Master File and preparation for relevant QC checks when applicable
• Tracking site budget related matters, including processing invoices, tracking payments and also for scheduling meetings, updating Excel trackers, coordinating the translation of site documents
• Producing study aids and clinical documentation

You are:

• An interest in the pharmaceutical industry and clinical research.
• At least 6 months' experience working within a similar role, happy to look at candidates from academia background and/or commercial
• A degree level qualification in Life Science, have equivalent experience or be a licensed healthcare professional.
• Fluent English, along with proficiency in the use of Microsoft Office suite is required.
• Office based at client site based in White City, London.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 through the form below.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.