Clinical Operations Analyst

Job Description

We seek a Clinical Operations Analyst to join our Chester-based team. This pivotal role involves supporting the management of clinical trials and ensuring compliance with regulatory standards. The ideal candidate will possess strong analytical skills and a passion for improving healthcare outcomes.

Responsibilities

• Contribute to the preparation of study budgets and timelines.
• Identify risks and challenges associated with ongoing trials.
• Collaborate with external partners and vendors as needed.
• Assist in conducting feasibility assessments for new studies.
• Maintain accurate records of trial-related documentation.

Requirements

Education

• Bachelor's degree in a relevant field
• PhD in a related discipline is preferred

Experience

• 3+ years of experience in clinical trial operations

Technical Skills

• Clinical Compliance Monitoring
• Project Management

Soft Skills

• Analytical Thinking
• Interpersonal Skills

Certifications

• Clinical Research Coordinator (CRC) Certification
• Regulatory Affairs Certification (RAC)

Languages

• English: Fluent

Advantageous

• Proficiency in project management software: Experience using tools like Asana or Trello in project planning.
• Knowledge of patient recruitment strategies: Experience in strategies for recruiting participants for clinical trials.

Benefits

• Comprehensive health insurance coverage
• Generous annual leave policy
• Training and professional development opportunities
• Employee assistance program for wellness support

Company Culture

• Inclusion: We strive for a diverse and inclusive workplace where everyone feels valued.
• Innovation: We encourage creative approaches and new ideas to drive progress.
• Work-Life Balance: We understand the importance of work-life balance and offer flexibility.