Study Coordinator: Own the Trial & Drive Delivery

Panthera Clinic; Preston; Hybrid; GBP 27,000 - 39,000; Full time

Benefits offered by this job

25 days leave + bank holidays

Life insurance 3x annual salary

Healthcare cash plan

Employee Assistance Programme

Electric Car Scheme

Annual Self-Care Day

Job summary

Panthera Biopartners in Preston is seeking a proactive Study Coordinator to manage day-to-day delivery of clinical studies at the site. You will own trackers, enrolment timelines and ensure study documentation is accurate while collaborating with clinical teams, monitors and vendors.

The role requires experience in clinical research, strong data-entry skills and the ability to prioritise multiple activities while maintaining compliance with regulatory requirements.

Qualifications

• Experience in clinical research or regulated environments.
• Ability to manage multiple study activities and timelines.
• Strong data-entry accuracy and deadline awareness.
• Good understanding of trial documentation and regulatory requirements.
• Excellent communication with study teams, monitors and vendors.

Responsibilities

• Take ownership of study trackers, timelines, enrolment and overall study progress.
• Lead day-to-day study coordination and ensure site readiness for key activities, including pre-randomisation.
• Coordinate communication between study teams, vendors, monitors and site colleagues.
• Maintain accurate study documentation (ISF, logs, EDC).
• Complete accurate data entry and support timely query resolution.
• Prepare for and support CRA monitoring visits.
• Support safety reporting (SAEs).
• Ensure studies are delivered in line with protocols and regulatory requirements.

Skills

Organised

Detail-oriented

Strong communication

Prioritisation

Time management

Tools

EDC systems

ISF management

Job description

Panthera Biopartners in Preston is seeking a proactive Study Coordinator to manage day-to-day delivery of clinical studies at the site. You will own trackers, enrolment timelines and ensure study documentation is accurate while collaborating with clinical teams, monitors and vendors.

The role requires experience in clinical research, strong data-entry skills and the ability to prioritise multiple activities while maintaining compliance with regulatory requirements.