Luton - Oncology CTA position

ICON Strategic Solutions; United Kingdom; Hybrid; GBP 150,000 - 200,000; Full time

Job summary

A leading clinical research organization in the UK is seeking an Oncology Senior Clinical Study Administrator in Luton. This role involves coordination and administration of clinical study activities, ensuring compliance with study deliverables, and engaging with various teams. A sciences degree and relevant clinical research experience are required. The position offers a competitive full-time salary and various benefits, including flexible working options.

Benefits

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualifications

• Relevant clinical research experience is preferred.
• Solid understanding of clinical research is required.
• Experience within the Pharmaceutical Industry is desirable.

Responsibilities

• Coordinate and administer clinical study activities.
• Ensure quality and consistency of study deliverables.
• Assist in the clinical trial application process.

Skills

Clinical research experience

Understanding of clinical trials

Communication skills

Ability to work in a fast-paced environment

Education

Sciences degree/equivalent

Job description

Luton UK - Oncology CTA position available

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

*Luton - office-based position available*

Here at the ICON Global Strategic Solutions team, we are looking to add a further employee to our growing group of experienced Senior Clinical Study Administrators in Luton. We are considering candidates with relevant clinical research experience and a solid understanding of clinical research.

You will be partnering with a well-known global pharmaceutical company with a strong portfolio in Oncology trials.

Responsibilities

You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.

The Oncology Senior Clinical Study Administrator assists in the coordination and administration of the clinical study activities in the study start-up team, and within the Local Study Team, ensures the quality and consistency of study deliverables to time, cost and quality objectives. - Reporting into the Clinical Administration Manager, you’ll be involved in the coordination and administration of clinical studies from the start-up to execution and close-out. For this post, it is desirable that you have similar clinical trial experience within the Pharmaceutical Industry.

You will be collecting, assisting in preparation, reviewing and tracking of documents for the clinical trial application process. You’ll contribute to the production and maintenance of study documents, and be template and version compliant.

Also, you will need to translate or give the appropriate support with the translation of documents when required. Working closely with the Project Leader and CRA teams, you will be working on a number of clinical studies at any one time. You need to be comfortable working in a fast-paced environment.

Sciences degree/equivalent.

• Permanent full-time contract of employment with us and 100% embedded to one client
• Office-based in the Luton area (England): minimum 3 days per week and 2 days working from home
• Competitive salary depending on level of skills and experience plus company benefits

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 maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

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, 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 or submit a request here

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.

Are you a current ICON Employee? Please click here to apply