Clinical Trial Associate

Job Description

As a Clinical Trial Associate in Chester, you will play a vital role in the management and coordination of clinical trials. This position will require meticulous attention to detail and knowledge of regulatory guidelines, as you support the successful execution of studies.

Responsibilities

• Collaborate with the clinical team to implement trial protocols.
• Track regulatory compliance and document management.
• Assist in the development of study-specific materials.
• Monitor patient safety and adverse event reporting.
• Participate in meetings to discuss study progress.
• Assist in budget management and financial tracking.
• Ensure the availability of study supplies.
• Contribute to risk assessment and management strategies.
• Help facilitate patient visits and follow-ups.
• Maintain a comprehensive understanding of the study objectives.

Requirements

Education

• Bachelor's degree in a scientific discipline
• Postgraduate qualification in Clinical Research is an advantage

Experience

• 2+ years of experience in clinical trials or research settings

Technical Skills

• Clinical Data Management
• Regulatory Submissions

Soft Skills

• Organizational Skills
• Adaptability

Certifications

• Certified Clinical Research Associate (CCRA)

Languages

• English: Fluent

Advantageous

• Knowledge of pharmacovigilance: Experience in monitoring drug safety and adverse reactions.
• Understanding of trial budgeting and finance: Knowledge of financial aspects related to clinical trials.

Benefits

• Generous annual leave policies
• Pension scheme with employer contributions
• Professional development budget
• Access to wellness programs

Company Culture

• Continuous Improvement: We prioritize learning and development opportunities for our team.
• Employee Empowerment: We empower our employees to take initiative and drive their success.