Snr Clinical Study Administrator - Luton

ICON Strategic Solutions; United Kingdom; Hybrid; GBP 30,000 - 50,000; Full time

Job summary

A leading global company in clinical research is seeking a Senior Clinical Study Administrator to join their Luton office. The role involves coordinating clinical studies, managing documents, and ensuring high-quality deliverables. Ideal candidates will have a background in clinical research and thrive in a fast-paced environment, contributing to impactful clinical trials.

Benefits

Competitive salary

Company benefits

Flexible working arrangements

Qualifications

• Relevant clinical trial experience within the Pharmaceutical Industry is desirable.
• Experience in preparing and reviewing clinical trial documents.
• Ability to work effectively as part of a team.

Responsibilities

• Assist in coordinating and administering clinical study activities.
• Ensure quality and consistency of study deliverables.
• Translate and support the document translation process when required.

Skills

Clinical research experience

Document management

Coordination skills

Fast-paced environment adaptability

Education

Sciences degree or equivalent

Job description

*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 a variety of clinical trials.

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 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

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.