Clinical Research Coordinator

Job Description

We are seeking a skilled Clinical Research Coordinator to join our Chester team. This role involves overseeing clinical trials, ensuring adherence to regulatory compliance, and managing participant recruitment. The ideal candidate has a strong background in clinical research and excellent organisational skills.

Responsibilities

• Lead the operational aspects of clinical trials.
• Conduct informed consent discussions with participants.
• Ensure timely collection and analysis of data.
• Support audit processes to ensure compliance.
• Engage with regulatory bodies to facilitate approval processes.
• Deliver training sessions on study protocols to research staff.
• Maintain relationships with external stakeholders.
• Contribute to the writing and submission of study protocols.

Requirements

Education

• Degree in Healthcare or Clinical Research
• Advanced degree preferred

Experience

• 4+ years of experience in clinical research

Technical Skills

• Clinical research protocols
• Statistical software

Soft Skills

• Leadership
• Interpersonal skills

Certifications

• Associate Clinical Research Coordinator (ACRC)
• Certified Clinical Research Associate (CCRA)

Languages

• English: Fluent

Advantageous

• Prior experience in a pharmaceutical environment: Experience working within a pharmaceutical company can be beneficial.
• Knowledge of biostatistics: Understanding of biostatistical principles as they apply to clinical research.

Benefits

• Enhanced salary package with additional bonuses.
• Access to professional development opportunities.
• Support for further education and certifications.
• Wellness programs to promote health and wellbeing.

Company Culture

• Inclusivity: We strive to create an inclusive workplace where everyone's contributions are valued.
• Learning and Development: We prioritise continuous professional development for our staff.