Location
London

Hours
Full Time

Salary
Competitive, commensurate with experience

About the Role
The Clinical Site Manager is responsible for managing clinical trial sites from site qualification through to site management, including data management, image quality control (QC), and query management as part of delivering Qureight’s imaging CRO services. You will coordinate site qualification activities such as site evaluation, training, and scanner qualification to ensure timely onboarding of priority clinical study sites. The role involves proactive site-facing communications to support sites in completing qualification activities before activation, managing post-qualification site activities including query resolution, and acting as the primary point of contact for assigned clinical sites. You will collaborate closely with data management colleagues to raise and resolve data queries and support image QC processes as needed. Additionally, you will track and report project and site milestones, maintain essential documentation, participate in clinical project kick-off meetings, and ensure all work complies with Good Clinical Practice (GCP), ISO27001, and data privacy regulations. This role requires building strong relationships with stakeholders at sites, sponsors, customers, and within Qureight, maintaining transparent and consistent communication. You will also contribute to continuous improvement and operational efficiency within Clinical Operations.

Experience
- Minimum of 1-2 years clinical trial site management experience is desirable but not essential
- Experience with clinical imaging modalities such as CT or MRI is desirable but not essential
- Demonstrated ability to cultivate and maintain key stakeholder relationships internally and externally
- Knowledge of ICH Good Clinical Practice (GCP) with evidence of recent training
- Experience working within a Quality Management System (QMS), e.g., ISO 9001, ISO 13485, is desirable
- Knowledge of relevant regulatory, compliance, and industry standards such as 21 CFR Part 11 is desirable

About you
- Strong organisational and time management skills with the ability to prioritise tasks effectively
- Strong interpersonal skills with high proficiency in written and verbal communication
- Proven track record of effective problem solving in a highly technical and innovative environment with good attention to detail
- Positive, can-do attitude with tenacity and drive to achieve objectives

Qualifications
- A relevant degree in life sciences or related field is desirable but not essential