Clinical Trials Study Coordinator — Drive Study Delivery

Panthera Bio; Lancashire; On-site; GBP 27,000 - 39,000; Full time

Benefits offered by this job

Annual leave

Leave buy/sell

Life insurance

Healthcare plan

Employee assistance

Sickness & family policies

Electric car scheme

Self-care day

Job summary

Panthera Biopartners is seeking an experienced Study Coordinator for our Preston site to manage day-to-day study delivery and ensure timely enrolment and progress. You will work with clinical teams, monitors and vendors to maintain high-quality documentation and data accuracy.

Responsibilities include ownership of study trackers, coordinating activities, and supporting monitoring visits and safety reporting, while ensuring compliance with protocols and regulatory requirements at a busy clinical

Qualifications

• Experience working in clinical research or regulated environment.
• Strong data-entry skills and attention to accuracy.

Responsibilities

• Take ownership of study trackers, timelines, enrolment and overall progress.
• Lead day-to-day study coordination and ensure site readiness for key activities.
• Coordinate communication between study teams, vendors, monitors and site colleagues.
• Maintain accurate study documentation including ISF, logs and EDC systems.
• Enter data accurately and support timely query resolution.
• Prepare for and support CRA monitoring visits.
• Support safety reporting including SAEs.
• Ensure studies adhere to protocols and regulatory requirements.

Skills

Clinical research

Data entry

Documentation

Regulatory knowledge

Communication

Prioritization

Job description

Panthera Biopartners is seeking an experienced Study Coordinator for our Preston site to manage day-to-day study delivery and ensure timely enrolment and progress. You will work with clinical teams, monitors and vendors to maintain high-quality documentation and data accuracy.

Responsibilities include ownership of study trackers, coordinating activities, and supporting monitoring visits and safety reporting, while ensuring compliance with protocols and regulatory requirements at a busy clinical