Clinical Operations Officer

Job Description

We are seeking a dedicated Clinical Operations Officer to manage and facilitate clinical trials in Chester. The candidate will oversee all aspects of operational efficiency, ensuring compliance with regulatory requirements and SOPs.

Responsibilities

• Coordinate all operational aspects of clinical studies, ensuring regulatory compliance.
• Develop and monitor project timelines, deliverables, and budget adherence.
• Facilitate cross-department collaboration to achieve project goals.
• Perform risk assessments and ensure mitigation strategies are in place.
• Ensure timely and accurate communication with project stakeholders.
• Assist in the preparation of clinical study reports and submissions to regulatory bodies.

Requirements

Education

• Bachelor's degree in Life Sciences, Medicine, or related field
• Master's degree in Clinical Research is an advantage

Experience

• 5+ years of experience in clinical trial operations

Technical Skills

• Clinical Project Management
• Quality Assurance

Soft Skills

• Leadership
• Analytical Skills

Certifications

• Clinical Research Coordinator (CRC) Certification
• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent

Advantageous

• Experience in pharmacovigilance: Knowledge and experience in monitoring drug safety.
• Health Economics and Outcomes Research (HEOR): Experience with HEOR methodologies and applications.

Benefits

• Attractive salary and performance bonuses
• Health and dental cover
• Flexible work arrangements
• Ongoing training and career development

Company Culture

• Collaboration: We believe in the power of teamwork and seek to build strong relationships within our organisation.
• Continuous Improvement: Encouraging feedback and continuous improvement is key to our operations.
• Supportive Environment: We strive to create a supportive environment for professional growth and personal development.