Global Clinical Site Lead – Imaging Trials

Qureight; Cambridge; On-site; GBP 65,000 - 90,000; Full time

Benefits offered by this job

Annual bonus

Private medical insurance

Life insurance

Cycle-to-work scheme

Pension scheme

Equity

Job summary

Qureight is seeking a Clinical Site Manager to oversee clinical trial sites from site qualification through ongoing management. You will coordinate onboarding, ensure QA compliance, and handle data queries in collaboration with data management teams.

You will build strong relationships with sites, sponsors, and internal stakeholders in a fast-moving imaging CRO environment. The role requires experience in site management and knowledge of GCP/quality standards, with an emphasis on timely

Qualifications

• Experience in clinical trial site management.
• Experience with clinical imaging is desirable but not essential.
• Knowledge of ICH GCP and GMP/ISO standards recommended.
• Ability to manage multiple sites and timelines.

Responsibilities

• Lead site qualification activities and onboarding of priority sites.
• Coordinate site communications to support qualification before activation dates.
• Manage site qualification and post-qualification activities including data queries.
• Raise and track data queries with site staff in collaboration with data management.
• Serve as primary contact for assigned sites and escalate as needed.
• Respond to and resolve inbound support requests per SOPs and SLA.
• Maintain project milestones and update internal systems with project data.
• Support image QC processes where required, in line with SOPs.
• Develop expertise in CT imaging and related regulatory requirements.

Skills

Clinical trial site management

Stakeholder relationships

GCP knowledge

Time management

Quality management systems

Regulatory compliance

Education

Life sciences degree

Job description

Qureight is seeking a Clinical Site Manager to oversee clinical trial sites from site qualification through ongoing management. You will coordinate onboarding, ensure QA compliance, and handle data queries in collaboration with data management teams.

You will build strong relationships with sites, sponsors, and internal stakeholders in a fast-moving imaging CRO environment. The role requires experience in site management and knowledge of GCP/quality standards, with an emphasis on timely