Global Clinical Site Manager – Imaging Trials

Qureight Ltd; Cambridge; Hybrid; GBP 45,000 - 65,000; Full time

Benefits offered by this job

Private medical insurance

Life insurance

Cycle-to-work scheme

Contributory pension scheme

Equity

Job summary

Qureight Ltd. is seeking a Clinical Site Manager to oversee trial sites from qualification through active management, including data and image QC tasks.

You will coordinate onboarding, maintain site communications, and ensure regulatory compliance under GCP standards. The role requires proven site-management experience, strong organizational skills, and the ability to work with cross-functional teams across sponsors and sites.

Qualifications

• Demonstrated experience in clinical trial site management.
• Experience with clinical imaging (CT or MRI) desirable.
• Strong organizational and time management skills.
• Ability to cultivate key stakeholder relationships.
• Knowledge of ICH GCP with recent training.
• Experience with a QMS (ISO 9001, ISO 13485) desirable.
• Knowledge of regulatory standards (e.g., 21 CFR Part 11) desirable.
• Excellent written and verbal communication.
• Can-do attitude with drive to achieve objectives.

Responsibilities

• Conduct site qualification activities and onboarding.
• Provide site-facing communications to support activation dates.
• Manage post-qualification site activities including queries.
• Raise data queries with site staff and drive to completion.
• Act as primary contact for assigned sites.
• Respond to inbound support requests per SOPs.
• Maintain stakeholder communications in a professional manner.
• Track milestones and update internal systems.
• Support image QC processes when needed.
• Develop CT knowledge and coordinate onboarding as needed.
• Maintain site-facing documents and share as needed.
• Participate in project kick-off meetings.
• Work in line with GCP and ISO27001 data privacy.
• Drive continuous improvements and operational efficiency.
• Build relationships with sponsors, customers, and Qureight teams.
• Support general Clinical Operations activities.

Skills

Clinical site management

Organisational skills

Time management

Stakeholder relations

Communication skills

GCP knowledge

QMS ISO 9001/13485

Regulatory knowledge 21 CFR Part 11

Problem solving

Can-do attitude

Education

Life sciences degree

Job description

Qureight Ltd. is seeking a Clinical Site Manager to oversee trial sites from qualification through active management, including data and image QC tasks.

You will coordinate onboarding, maintain site communications, and ensure regulatory compliance under GCP standards. The role requires proven site-management experience, strong organizational skills, and the ability to work with cross-functional teams across sponsors and sites.