ChesterFull-time£45,000 - £60,000 / Year (£3,750 - £5,000 / Month)
Job Description
We are seeking a Clinical Trials Manager to oversee our clinical trial operations in Chester. The successful candidate will manage all aspects of trial execution, from planning to implementation, ensuring compliance with regulations and timelines.
Responsibilities
Directly supervise clinical trial operations from design to closeout.
Ensure adherence to GCP and safety regulations throughout the trial.
Manage the clinical trial budget and expenses efficiently.
Act as the primary point of contact for trial-related queries.
Facilitate communication among cross-functional teams.
Conduct site visits to ensure compliance and quality standards.
Analyze data and provide insights for study actions.
Review clinical trial protocols and informed consent forms.
Identify and implement process improvements for trial efficiency.
Prepare comprehensive reports for submission to regulatory bodies.
Requirements
Education
Bachelor's degree in Health Sciences or relevant field
Master's degree in Public Health or Clinical Research is advantageous
Experience
5+ years in clinical operations or relevant experience
Technical Skills
Clinical trial design
Project management
Patient recruitment strategies
Soft Skills
Analytical thinking
Interpersonal skills
Certifications
International Conference on Harmonisation (ICH) Training
Languages
English: Fluent
Advantageous
Proficient in project management software: Experience using tools like MS Project or Trello for tracking project progress.
Familiarity with remote monitoring technologies: Experience with technologies for remote patient monitoring.
Benefits
Attractive salary with annual bonus potential
Work-life balance initiatives
Health, dental, and vision insurance
Continued education and training support
Company Culture
Collaboration: We foster teamwork and encourage ideas from all levels of the organisation.
Diversity and Inclusion: We celebrate diversity and strive to create an inclusive workplace.