Patient-Centric Clinical Research Coordinator

Civia Health; Brighton; On-site; GBP 40,000 - 60,000; Full time

Job summary

A healthcare research organization in Brighton is looking for a Clinical Research Coordinator to manage clinical trials, ensuring ethical and patient-centered practices. Ideal candidates will have a degree in health sciences, possess excellent organizational skills, and have experience in coordinating clinical studies. This position offers competitive compensation, professional development, and a mission-driven, collaborative work environment.

Benefits

Competitive compensation

Medical, dental, and vision insurance

Generous PTO and paid holidays

Flexible scheduling options

Professional development support

Qualifications

• Minimum 3 years of experience coordinating Phase 2–4 clinical trials.
• Experience with eSource and eConsent systems preferred.
• Knowledge of GCP, FDA regulations, and clinical trial conduct.

Responsibilities

• Coordinate and manage all aspects of assigned clinical trials.
• Conduct study visits and obtain informed consent.
• Recruit and enroll study participants according to protocol.

Skills

Interpersonal skills

Organizational skills

Attention to detail

Collaboration

Education

Bachelor’s degree in health sciences or related field

Tools

Microsoft Office Suite

Clinical trial management systems

eSource systems

Job description

A healthcare research organization in Brighton is looking for a Clinical Research Coordinator to manage clinical trials, ensuring ethical and patient-centered practices. Ideal candidates will have a degree in health sciences, possess excellent organizational skills, and have experience in coordinating clinical studies. This position offers competitive compensation, professional development, and a mission-driven, collaborative work environment.