Clinical Operations Supervisor

Job Description

We are seeking a Clinical Operations Supervisor to manage and oversee clinical research projects in Chester. The ideal candidate will have experience in coordinating clinical trials and will ensure compliance with regulatory standards.

Responsibilities

• Plan, initiate, and oversee clinical studies to ensure deliverables meet quality standards.
• Evaluate potential clinical sites and negotiate contracts.
• Tender expert guidance to ensure operational efficiency across trial phases.
• Generate comprehensive reports and presentations for senior management.
• Simultaneously manage multiple projects while ensuring data integrity and patient safety.

Requirements

Education

• Bachelor's degree in Health Sciences or equivalent
• Master's degree in Clinical Research is beneficial

Experience

• 5+ years of experience in clinical trial management

Technical Skills

• Clinical Operations
• Budget Management

Soft Skills

• Team Management
• Interpersonal Skills

Certifications

• Certified Clinical Research Associate (CCRA)
• Certified Clinical Research Coordinator (CCRC)

Languages

• English: Fluent

Advantageous

• Knowledge of statistical analysis software: Experience working with software like SAS or SPSS.
• Experience with remote monitoring techniques: Knowledge of remote monitoring in clinical trials.

Benefits

• Comprehensive health and dental insurance
• Flexible working hours with remote options available
• Professional development opportunities
• Access to mental health resources

Company Culture

• Continuous Professional Development: We facilitate continuous learning opportunities and professional growth for all staff members.
• Work-Life Balance: We promote a healthy work-life balance, ensuring that employees feel supported both personally and professionally.