Clinical Trial Coordinator

Peterborough FULL TIME £30,000 - £40,000 / Year
(£2,500 - £3,333 / Month)

Job Description

We are looking for an experienced Clinical Trial Coordinator to manage various aspects of clinical trials, ensuring compliance with regulations and protocols. The ideal candidate will excel in coordinating between different stakeholders and maintaining documentation.

Responsibilities

  • Supervise site visits and ensure protocols are followed accurately.
  • Maintain familiarity with clinical trial best practices and regulations.
  • Assist in developing trial-specific training materials.
  • Respond to inquiries from investigators and sponsors regarding trial issues.
  • Evaluate site performance and address any issues proactively.

Requirements

Education
  • Bachelor's degree in Pharmacy or related field
  • Advanced degree in Clinical Research is a plus
Experience
  • 3+ years of experience in clinical trial management
Technical Skills
  • Statistical analysis software
  • Familiarity with Electronic Data Capture (EDC) systems
Soft Skills
  • Problem-solving abilities
  • Interpersonal skills
Certifications
  • Certified Clinical Research Coordinator (CCRC)
  • Good Clinical Practice (GCP) Certification
Languages
  • English: Fluent

Advantageous

  • Knowledge of therapeutic areas: Experience in oncology, cardiology, or rare diseases is beneficial.
  • Project management skills: Ability to manage clinical trial projects from inception to completion.

Benefits

  • Comprehensive health and wellness benefits
  • Generous holiday entitlement
  • Flexible working arrangements
  • Training and career advancement opportunities

Company Culture

  • Innovation: We encourage innovative thinking and creative problem-solving within our teams.
  • Work-Life Balance: We prioritise a healthy work-life balance through flexible working policies and supportive management.
  • Community Engagement: We are committed to making a positive impact in the communities we serve.
Status: Closed