Clinical Research Coordinator

Job Description

We are seeking a passionate and skilled Clinical Research Coordinator to join our team in Newcastle. The ideal candidate will be responsible for overseeing clinical trials, ensuring compliance with regulatory requirements, and managing day-to-day operations of research projects.

Responsibilities

• Lead the preparation and submission of Investigator's Brochures and study protocols to ethics committees.
• Coordinate with laboratories, imaging facilities, and other service providers.
• Provide guidance and support to clinical staff on study-related issues.
• Organize and participate in study meetings and conferences.
• Assist in drafting publications and presentations based on study outcomes.
• Evaluate and monitor sites for compliance and performance.
• Support the establishment of quality assurance protocols.
• Implement corrective actions to resolve compliance issues.

Requirements

Education

• Bachelor's degree in a relevant scientific discipline
• Master's in Public Health or Clinical Research is an advantage

Experience

• 3+ years of experience in clinical settings

Technical Skills

• Familiarity with clinical trial management software
• Statistical analysis

Soft Skills

• Attention to detail
• Adaptability

Certifications

• Certified Clinical Research Coordinator (CCRC)
• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent

Advantageous

• Experience with patient recruitment strategies: Knowledge of effective methods for recruiting participants in clinical trials.
• Experience in budget management: Capabilities in managing budgets for clinical research projects.

Benefits

• Pension scheme with employer contributions
• Flexible working options
• Employee assistance programs
• Support for continuing education and training

Company Culture

• Support: We provide a supportive work environment with mentorship and training opportunities.
• Diversity: We value diverse backgrounds and perspectives, promoting inclusivity within our team.