Clinical Trials Analyst

Job Description

As a Clinical Trials Analyst, you will play a crucial role in the execution of clinical trials, ensuring compliance with regulatory standards and quality assurance protocols. You will work collaboratively with clinical teams to manage study timelines, data collection, and reporting.

Responsibilities

• Oversee day-to-day operations of clinical trials.
• Ensure all trial activities align with regulatory standards.
• Evaluate and report on site performance and data integrity.
• Maintain trial master files and documentation.
• Communicate effectively with all study stakeholders.
• Collaborate with multidisciplinary teams to drive project success.
• Utilize statistical methods for data analysis and interpretation.

Requirements

Education

• Bachelor's degree in a relevant scientific field
• Postgraduate qualifications are beneficial

Experience

• 3+ years of experience in clinical trials or research

Technical Skills

• Regulatory Knowledge
• Project Management

Soft Skills

• Critical Thinking
• Teamwork

Certifications

• Clinical Research Associate (CRA)
• GCP Certification

Languages

• English: Fluent

Advantageous

• Familiarity with electronic data capture (EDC) systems: Experience in managing data capture through electronic systems.
• Knowledge of patient recruitment strategies: Skills in developing and implementing patient recruitment strategies.

Benefits

• Generous annual leave entitlement
• Pension scheme with company matching
• Regular team-building events and activities
• Access to wellness programmes

Company Culture

• Diversity and Inclusion: Our team is diverse and inclusive, and we value the unique contributions of every member.
• Continuous Improvement: We are committed to continuous improvement and learning, ensuring our team grows together.
• Patient-Centric Approach: Our work revolves around improving patient outcomes and enhancing healthcare solutions.