Clinical Research Scientist

Job Description

As a Clinical Research Scientist at our Chester facility, you will play a pivotal role in designing and executing clinical trials. You will work closely with multidisciplinary teams to ensure compliance with regulatory standards while delivering high-quality data that drives innovative healthcare solutions.

Responsibilities

• Oversee the recruitment and consent of study participants.
• Assist in budget preparation and resource allocation for clinical trials.
• Review literature to inform clinical study design.
• Prepare regulatory submissions for study approval.
• Supervise research assistants in data collection and entry.

Requirements

Education

• PhD in Clinical or Health Sciences
• Postdoctoral experience is advantageous

Experience

• 5+ years of experience in clinical research studies

Technical Skills

• Clinical research methodologies
• Data management systems

Soft Skills

• Teamwork
• Communication

Certifications

• Certified Clinical Research Coordinator (CCRC)
• Project Management Professional (PMP)

Languages

• English: Fluent

Advantageous

• Proficiency in project management tools: Experience using project management software to track study progress.
• Familiarity with electronic health records (EHR): Knowledge of EHR systems for data collection and management in clinical settings.

Benefits

• Full health, dental, and vision coverage
• Training and professional development opportunities
• Employee assistance programmes
• Team-building activities and social events

Company Culture

• Continuous Improvement: We are always striving for improvement, encouraging our staff to pursue ongoing professional development.
• Diversity and Inclusion: Our team values diversity and strives to create an inclusive environment for all employees.
• Recognition: We celebrate successes and recognise the contributions of all team members.