Site Care Partner – Oncology
Posted 18hrs ago
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Job Description
Site Care Partner supporting UK oncology clinical trials for Parexel, a global clinical development partner. Managing investigator sites from start-up through closeout while ensuring compliance and recruitment performance.
Responsibilities:
- Lead site start-up and activation activities, including site qualification, pre-trial assessments, site initiation activities, and activation readiness
- Support country and site selection processes with local intelligence, feasibility insights, and site assessment input
- Build and maintain relationships with investigator sites throughout the study lifecycle
- Serve as the operational point of contact for site-level questions and coordinate issue resolution
- Ensure completion of required training, documentation, and systems activities for site activation and study execution
- Drive site recruitment planning and enrolment support
- Communicate regularly with sites to monitor study progress, recruitment performance, and operational deliverables
- Review site monitoring reports and support compliance with informed consent documentation and amendments
- Oversee site-related deliverables, including data entry, data review, database lock readiness, and investigator documentation
- Identify quality, compliance, and operational risks and implement mitigation plans
- Support decentralized trial capabilities and adoption of study technologies and processes
- Collaborate with internal stakeholders to optimize communication, site experience, and study delivery outcomes
Requirements:
- Bachelor’s degree, Registered Nurse qualification, or equivalent combination of education, training, and experience
- At least 5 years of experience in clinical research, site management, monitoring, or a related field
- Demonstrated experience in site management with prior experience as a Site Monitor
- Demonstrated experience across the full clinical trial lifecycle, from study start-up and site activation through closeout
- Knowledge of ICH GCP, applicable regulatory requirements, and clinical trial processes
- Experience with clinical trial systems such as EDC, Shared Investigator Platform, Site Profile, or similar clinical research technologies
- Strong relationship building, stakeholder management, communication, organizational, and problem solving skills
- Ability to collaborate effectively across cross functional and geographically diverse teams
- Patient focused mindset with strong attention to quality, compliance, and operational excellence
- Comfort working with clinical trial systems, study oversight processes, and site management activities
- Ability to travel regularly throughout the UK, up to 50%
- Proficiency in English
Benefits:
- Medical & Dental Insurance
- Life Assurance
- Pension
- Critical Illness Insurance & Health Screenings
- Comprehensive benefits package for eligible employees
- Flexible work arrangements
- Career growth opportunities

















