Clinical Research Associate

Job Description

We are currently seeking a Clinical Research Associate to join our Liverpool team. The ideal candidate will be responsible for overseeing clinical trials, ensuring compliance with protocol, and liaising with various stakeholders. This role offers a unique opportunity to contribute to important medical research that can change lives.

Responsibilities

• Lead site initiation visits and ensure all study materials are in place.
• Collaborate with data management teams to ensure data quality and accuracy.
• Assist in the development of study-specific materials such as protocols and patient consent forms.
• Provide feedback and recommendations for process improvements.
• Facilitate regular meetings with study teams to discuss progress and issues.
• Document and follow up on study events and adverse reactions.

Requirements

Education

• Bachelor's degree in Biomedical Sciences or a relevant field
• Master's degree in Clinical Research is preferable

Experience

• 1-3 years of clinical research experience, preferably in a CRA role

Technical Skills

• Patient Interaction
• Project Coordination

Soft Skills

• Problem Solving
• Time Management

Certifications

• Clinical Research Coordinator (CRC) Certification
• Basic Life Support (BLS) Certification

Languages

• English: Fluent

Advantageous

• Knowledge of pharmacovigilance: Experience in monitoring drug safety and adverse reactions.
• Familiarity with clinical trial software: Proficiency with various clinical trial management systems.

Benefits

• Comprehensive health insurance coverage
• Retirement savings plan with employer match
• Paid time off and holidays
• Access to ongoing training and career advancement

Company Culture

• Diversity and Inclusion: We believe in building a diverse workforce that reflects the communities we serve.
• Employee Wellbeing: Our company prioritises employee wellbeing and work-life balance.
• Excellence: We strive for excellence in our research and clinical practices.