Clinical Trials Coordinator

Job Description

We are seeking a detail-oriented Clinical Trials Coordinator to manage and support clinical research initiatives in Bristol. The ideal candidate will have experience in coordinating clinical trials and a passion for advancing healthcare.

Responsibilities

• Develop and implement trial protocols and standard operating procedures.
• Coordinate logistics for trial supplies and equipment.
• Evaluate eligibility and monitor participant retention.
• Work closely with statisticians and data managers on study design.
• Attend and participate in clinical trial meetings and presentations.
• Assist in maintaining trial budgets and timelines.
• Ensure compliance with local, national, and international regulations.

Requirements

Education

• Bachelor's degree in Health Sciences or a related field
• Postgraduate qualification in Clinical Research is favourable

Experience

• 3-5 years of experience managing clinical trials or research projects

Technical Skills

• Familiarity with clinical trial software
• Statistical analysis skills

Soft Skills

• Problem-solving abilities
• Attention to detail

Certifications

• Clinical Research Associate (CRA) Certification
• ISO 14155 Certified

Languages

• English: Fluent

Advantageous

• Previous experience in a laboratory setting: Background in a lab environment relevant to clinical research.
• Understanding of pharmacovigilance: Knowledge of safety monitoring and reporting requirements in clinical trials.

Benefits

• Flexible working hours and remote work options
• Health and wellness programs
• Pension scheme with employer contributions
• Work-life balance initiatives

Company Culture

• Continuous Learning: We encourage ongoing learning and professional development to support your career growth.
• Employee Recognition: Our company celebrates achievements and recognizes hard work, fostering employee satisfaction.
• Work-Life Balance: We understand the importance of work-life balance and offer flexible arrangements to support it.