Clinical Research Coordinator

Job Description

We are seeking a Clinical Research Coordinator to oversee and manage clinical trials in Chester. The ideal candidate will possess strong organizational skills, a keen attention to detail, and experience in clinical research protocols.

Responsibilities

• Develop and implement standard operating procedures for clinical trials.
• Act as the primary point of contact for study sponsors and stakeholders.
• Monitor clinical trial progress and address any issues that arise promptly.
• Assist with the preparation of study reports and publications.
• Ensure participant safety and well-being throughout the trial process.

Requirements

Education

• Bachelor's degree in a relevant field (biomedicine, healthcare)
• Postgraduate qualifications in clinical research is a plus

Experience

• 3+ years of experience as a Clinical Research Coordinator

Technical Skills

• Proficiency in clinical trial management software
• Strong analytical skills

Soft Skills

• Leadership
• Organizational skills

Certifications

• Clinical Research Associate Certification

Languages

• English: Fluent

Advantageous

• Technical writing skills: Ability to document protocols, reports, and correspondence effectively.
• Experience with remote trial participation: Understanding of virtual trial methodologies is an advantage.

Benefits

• Pension scheme with employer contributions
• Flexible working hours and remote work options
• Employee assistance programs and mental health support
• Annual team-building retreats and social events

Company Culture

• Commitment to Excellence: Our relentless pursuit of excellence drives us to improve processes and outcomes constantly.
• Learning and Growth: We provide continuous learning opportunities to help our team members grow and succeed.
• Employee Wellbeing: We prioritize the wellbeing of our employees through various support initiatives.