Senior Clinical Study Manager — Imaging Trials (Hybrid)

Qureight Ltd; Cambridge; Hybrid; GBP 70,000 - 110,000; Full time

Benefits offered by this job

Annual bonus

Private medical insurance

Life insurance

Cycle-to-work scheme

Contributory pension

Job summary

Qureight Ltd is seeking a Senior Clinical Study Manager to join our Clinical Operations team in a hybrid role based in Cambridge or London. You will lead study start-up and ongoing management, acting as the primary contact for customers and internal teams and ensuring delivery on time and to high quality.

Responsibilities include developing study plans, timelines and documents, managing risks, coordinating with site managers and data managers, and maintaining strong client relationships while

Qualifications

• Minimum 4 years of clinical research experience in imaging or related trials.
• Proven project manager experience in clinical research and study delivery.
• Strong knowledge of ICH GCP and regulatory standards (ISO 9001/13485).
• Excellent stakeholder management and communication skills.

Responsibilities

• Take overall responsibility for the operational delivery of studies from initiation to close-out.
• Lead client meetings, write key study documents, and manage milestones and risks.
• Coordinate with site managers, data managers, and cross-functional teams to ensure quality and timelines.
• Oversee financial aspects, forecasting, invoicing, and change governance.
• Maintain compliance with GCP, ISO standards, data privacy, and relevant regulations.

Skills

Clinical research

Project management

Regulatory knowledge

GCP familiarity

Stakeholder management

ISO 9001

ISO 13485

21 CFR Part 11

Job description

Qureight Ltd is seeking a Senior Clinical Study Manager to join our Clinical Operations team in a hybrid role based in Cambridge or London. You will lead study start-up and ongoing management, acting as the primary contact for customers and internal teams and ensuring delivery on time and to high quality.

Responsibilities include developing study plans, timelines and documents, managing risks, coordinating with site managers and data managers, and maintaining strong client relationships while