Paediatric Clinical Trials Data Coordinator

NHS; Sutton; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading healthcare provider is seeking a Clinical Data Coordinator in Sutton to support critical research initiatives in paediatric oncology. The role requires strong administrative and organisational skills, alongside experience in database management. Candidates will be involved in data collection, managing trial documentation, and ensuring compliance with clinical regulations. The successful applicant will join a supportive team and gain opportunities for professional development in a vital research area.

Benefits

Professional development opportunities

Qualifications

• Strong administrative and organisational skills.
• Experience in database management for clinical research.
• Knowledge of clinical trials and regulatory standards.

Responsibilities

• Data collection for paediatric cancer clinical trials.
• Managing trial administration and documentation.
• Ensuring compliance with Good Clinical Practice (GCP) guidelines.
• Collaborating with research team to support trial operations.

Skills

Administrative skills

Organisational skills

Database management

Knowledge of clinical trials

Job description

Job Title & Location

Clinical Data Coordinator • Sutton, England, GB

Overview

A leading healthcare provider is seeking a Clinical Trials Administrator in Sutton to support paediatric cancer research. Candidates should have strong administrative and organisational skills, experience in databases, andزع knowledge of clinical trials and regulations. The role involves data collection, managing trial administration, and ensuring compliance with GCP guidelines. Successful applicants will enjoy a supportive team environment and opportunities for professional development, contributing to vital research initiatives in paediatric oncology.

Responsibilities

• Data collection for paediatric cancer clinical trials
• Managing trial administration and documentation
• Ensuring compliance with Good Clinical Practice (GCP) guidelines(seg)
• Collaborating with research team to support trial operations

Qualifications

• Strong administrative and organisational skills
• Experience in database management for clinical research
• Knowledge of clinical trials and regulatory standards