Senior Clinical Study Administrator - Luton On-Site

3M HEALTHCARE; Greater London; Hybrid; GBP 42,000 - 56,000; Full time

Job summary

Parexel is seeking a Senior Clinical Study Administrator to join our UK team. The role focuses on coordinating and administering clinical studies from start-up through to close-out, ensuring quality and timely delivery.

You will be the local contact, supporting CRAs and trial managers across systems like CTMS and eTMF. The position requires a degree, strong organizational skills, IT proficiency, and fluency in English and French.

Qualifications

• Degree or equivalent in life sciences or a related field.
• Excellent written and spoken English.
• Fluent in French.

Responsibilities

• Coordinate clinical studies from start-up to execution and close-out within the local study team.
• Serve as the local administrative contact; collaborate with CRAs and trial managers.
• Set up and maintain information in CTMS/SharePoint and other systems.
• Manage study materials, equipment, and regulatory documents; support audits and inspections.
• Prepare meeting materials and liaise with sponsors, investigators, and vendors.

Skills

English proficiency

French language

Education

Bachelor's degree or equivalent

Job description

Parexel is seeking a Senior Clinical Study Administrator to join our UK team. The role focuses on coordinating and administering clinical studies from start-up through to close-out, ensuring quality and timely delivery.

You will be the local contact, supporting CRAs and trial managers across systems like CTMS and eTMF. The position requires a degree, strong organizational skills, IT proficiency, and fluency in English and French.