Clinical Study Operations Coordinator

AstraZeneca GmbH; Luton; On-site; GBP 32,000 - 52,000; Full time

Job summary

AstraZeneca is seeking a Clinical Study Administrator to support study leaders and cross-functional teams, ensuring logistics, confidentiality and accuracy across studies. You will contribute to audit readiness and compliant study administration, enabling researchers to advance trial delivery with confidence.

In this role you will collaborate globally, manage administrative tasks, drive continuous improvement, and help deliver timely decisions in an oncology-focused environment.

Qualifications

• High School Diploma or GED; 2+ years in Drug Development preferred.
• Bachelor’s degree preferred; 5+ years administrative experience.
• Experience in a Pharmaceutical/Drug Development environment.
• Professional qualification in administrative skills.
• Excellent time management and organizational skills.
• Ability to work independently with general guidance and adapt to changing priorities.

Responsibilities

• Manage study logistics, confidentiality and accuracy for study leaders and teams.
• Set up and follow-up on study-related contracts and purchase orders.
• Resolve administrative issues and maintain study momentum.
• Collaborate with global colleagues to align ways of working across countries and time zones.
• Advise on efficient administrative tasks and process improvements.
• Administer essential IS/IT systems to maintain data integrity across studies.
• Prepare and coordinate training and development for administrators and study support staff.
• Plan and coordinate events/small projects to support study execution.

Skills

Study coordination

Document management

Time management

Communication skills

Discretion and judgment

Independent work

Education

Bachelor's Degree

High School Diploma acceptable

Tools

Administrative systems

Job description

AstraZeneca is seeking a Clinical Study Administrator to support study leaders and cross-functional teams, ensuring logistics, confidentiality and accuracy across studies. You will contribute to audit readiness and compliant study administration, enabling researchers to advance trial delivery with confidence.

In this role you will collaborate globally, manage administrative tasks, drive continuous improvement, and help deliver timely decisions in an oncology-focused environment.