Site Care Partner – Oncology

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Lead activities for site start-up and activation, encompassing site qualification, pre-trial assessments, site initiation tasks, and readiness for activation.

• Assist in the processes for country and site selection by providing local insights, feasibility data, and input for site assessments.

• Establish and sustain relationships with investigator sites throughout the duration of the study.

• Act as the primary operational contact for site-related inquiries and coordinate the resolution of issues.

• Ensure the completion of necessary training, documentation, and system activities required for site activation and execution of the study.

• Drive planning for site recruitment and provide support for enrolment.

• Maintain regular communication with sites to track study progress, recruitment performance, and operational deliverables.

• Review site monitoring reports and assist in ensuring compliance with informed consent documentation and amendments.

• Oversee site-related deliverables such as data entry, data review, readiness for database lock, and documentation from investigators.

• Identify risks related to quality, compliance, and operations, and implement plans to mitigate them.

• Support capabilities for decentralized trials and the adoption of study-related technologies and processes.

• Collaborate with internal stakeholders to enhance communication, improve site experience, and achieve favorable study delivery outcomes.

⛳️ Requirements

• Bachelor’s degree, Registered Nurse qualification, or an equivalent combination of education, training, and experience.

• A minimum of 5 years of experience in clinical research, site management, monitoring, or a related area.

• Proven background in site management with prior experience as a Site Monitor.

• Demonstrated experience across the entire clinical trial lifecycle, from study start-up and site activation to closeout.

• Knowledge of ICH GCP, relevant regulatory standards, and clinical trial processes.

• Familiarity with clinical trial systems such as EDC, Shared Investigator Platform, Site Profile, or similar clinical research technologies.

• Strong skills in relationship building, stakeholder management, communication, organization, and problem-solving.

• Ability to work collaboratively across cross-functional and geographically diverse teams.

• A patient-focused mindset with a keen attention to quality, compliance, and operational excellence.

• Comfort in working with clinical trial systems, study oversight processes, and site management tasks.

• Willingness to travel regularly throughout the UK, up to 50% of the time.

• 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.