Clinical Trial Coordinator: Fast-Paced, Impact-Driven Role

Actalent; Warwick; On-site; GBP 26,000 - 38,000; Full time

Job summary

Actalent in the United Kingdom is seeking a Clinical Research Coordinator to support the delivery of innovative clinical studies. The role requires prior clinical research experience, strong organisation and communication skills, and the ability to manage multiple priorities while ensuring GCP compliance.

You will coordinate trial activities from start-up through close-out, assist with regulatory submissions and data entry, and act as a primary contact for participants, investigators and

Qualifications

• Understanding of ICH-GCP guidelines and trial processes.
• Experience with study documentation and data collection.
• Excellent organisational and communication skills.
• Ability to manage multiple priorities and meet deadlines.

Responsibilities

• Coordinate day-to-day clinical trial activities from start-up to close-out.
• Support participant recruitment, screening and enrolment.
• Schedule study visits and maintain study documentation.
• Ensure files comply with GCP and regulatory requirements.
• Collect, review and enter study data with accuracy.
• Support monitoring visits, audits and inspections.
• Assist with regulatory submissions and essential document management.
• Act as a key contact between participants, investigators, sponsors and vendors.
• Track study progress and assist with milestone delivery.

Skills

ICH-GCP knowledge

Clinical trial coordination

Data collection

Regulatory submissions

Communication skills

Education

Bachelor's degree in Life Sciences or related field

Job description

Actalent in the United Kingdom is seeking a Clinical Research Coordinator to support the delivery of innovative clinical studies. The role requires prior clinical research experience, strong organisation and communication skills, and the ability to manage multiple priorities while ensuring GCP compliance.

You will coordinate trial activities from start-up through close-out, assist with regulatory submissions and data entry, and act as a primary contact for participants, investigators and