Site Care Partner, Lead CRA, Oncology

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

📋 Description

• Oversee site start-up and activation processes, encompassing site qualification, pre-trial evaluations, initiation activities, and readiness for activation.

• Assist in country and site selection by leveraging local insights, feasibility data, and site assessment contributions.

• Cultivate and sustain relationships with investigator sites throughout the entire study duration.

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

• Ensure the timely completion of training, documentation, and system-related tasks necessary for site activation and study implementation.

• Propel site recruitment strategies and offer support for enrollment efforts.

• Track study progress, recruitment metrics, and operational deliverables through consistent communication with sites.

• Evaluate site monitoring reports and assist in maintaining compliance with informed consent documentation and any amendments.

• Supervise site deliverables, including data entry, data review, database lock preparedness, and investigator documentation.

• Detect quality, compliance, and operational risks while executing mitigation strategies.

• Facilitate decentralized trial capabilities and the integration of study technologies and processes.

• Partner with internal stakeholders to enhance site experiences and improve study delivery results.

• Support investigative sites throughout the clinical study lifecycle, from start-up and activation to conduct and closure.

⛳️ Requirements

• Bachelor’s degree, Registered Nurse qualification, or a comparable mix of education, training, and experience.

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

• Proven expertise in site management with prior roles as a Site Monitor/CRA.

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

• Familiarity with ICH GCP, relevant regulatory requirements, and clinical trial methodologies.

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

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

• Ability to collaborate effectively across cross-functional and geographically diverse teams.

• Patient-centric approach with a keen focus on quality, compliance, and operational excellence.

• Comfortable working with clinical trial systems, study oversight processes, and site management functions.

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

• Proficient in English.

🏝️ Benefits

• Medical & Dental Insurance.

• Life Assurance.

• Pension.

• Critical Illness Insurance & Health Screenings.

• Comprehensive benefits package for eligible employees.

• Flexible work arrangements.

• Opportunities for growth.