Snr Clinical Study Administrator - Luton

Symphony Health; London; Hybrid; GBP 35,000 - 50,000; Full time

Job summary

A leading company in pharmaceutical services is seeking a Senior Clinical Study Administrator in Luton. This role involves coordinating clinical study activities and ensuring compliance with regulatory standards. Candidates with experience in clinical trials and a science degree are encouraged to apply to join a team driven by innovation and excellence.

Benefits

Company benefits

Qualifications

• Candidates should have relevant clinical research experience.
• A solid understanding of clinical research practices is essential.

Responsibilities

• Coordinate and administer clinical studies from start-up through execution and close-out.
• Collect, prepare, review, and track documents for clinical trial applications.
• Manage multiple clinical studies simultaneously in a fast-paced environment.

Skills

Clinical research

Project management

Documentation management

Education

Science degree or 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 clinical study activities within the study start-up team and the Local Study Team, ensuring the quality and timeliness of study deliverables regarding scope, budget, and quality standards. Reporting to the Clinical Administration Manager, you will coordinate and administer clinical studies from start-up through execution and close-out. It is desirable that candidates have similar clinical trial experience within the pharmaceutical industry.

You will be responsible for collecting, assisting in the preparation, reviewing, and tracking of documents for the clinical trial application process. You will contribute to the production and maintenance of study documents, ensuring compliance with templates and version control.

Additionally, you will support document translation when required. Working closely with the Project Leader and CRA teams, you will manage multiple clinical studies simultaneously. The role requires comfort working in a fast-paced environment.

Qualifications

• Science degree or equivalent.
• Permanent full-time contract with ICON, embedded with one client.
• Office-based in the Luton area (England): minimum 3 days per week in the office and 2 days remote work.
• Competitive salary depending on skills and experience, plus company benefits.

At ICON, inclusion and belonging are fundamental to our culture and values. We are committed to providing an inclusive and accessible environment for all candidates. ICON promotes a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.