Snr Clinical Study Administrator - Luton

Pharmaceutical Research Associates, Inc; London; On-site; GBP 30,000 - 50,000; Full time

Job summary

Join a leading global team in a Senior Clinical Study Administrator role based in Luton. You will play a crucial part in managing clinical trials, ensuring high quality and compliance while working in a dynamic and supportive environment. This position offers a permanent full-time contract with opportunities for professional growth and a focus on innovation.

Benefits

Competitive salary based on experience

Company benefits

Flexibility with remote work

Qualifications

• Relevant clinical research experience is essential.
• Experience in coordinating clinical studies preferred.
• Ability to manage documentation and adhere to quality guidelines.

Responsibilities

• Assist in coordination and administration of clinical study activities.
• Collect, prepare, and track documents for the clinical trial application process.
• Support translation of documents when required.

Skills

Clinical research experience

Coordination and administration

Document management

Education

Sciences degree/equivalent

Job description

Overview

*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.

Responsibilities

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.

Qualifications

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.