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