Study Coordinator

Role overview

Key responsibilities

• Own study trackers, timelines, enrolment and overall study progress.
• Lead day-to-day coordination and prepare the site for key study activities.
• Coordinate communication between study teams, vendors, monitors and site colleagues.
• Maintain Investigator Site Files, study logs and electronic data capture records.
• Complete data entry and support query resolution.
• Prepare for and support CRA monitoring visits.
• Support Serious Adverse Event reporting.
• Ensure studies follow protocols, regulatory requirements and site procedures.

Requirements

• Have previous experience in clinical research or a similar regulated environment.
• Have experience coordinating clinical studies and maintaining study documentation.
• Have strong data-entry skills and excellent accuracy and deadline management.
• Understand clinical trial documentation and regulatory requirements.
• Communicate effectively with colleagues, monitors and external partners.
• Prioritise effectively and keep studies moving forward.

Workplace

• This is a site-based role at a Panthera clinical research site.
• There may occasionally be a requirement to support other local Panthera sites.

Compensation and benefits

• Salary is stated as £27,300 to £38,850; the pay cadence is not specified.
• Benefits include 25 days annual leave plus bank holidays, life insurance, a healthcare cash plan and an Employee Assistance Programme.
• Additional benefits include an annual leave purchase scheme, family-friendly policies, an electric car scheme and an annual self-care day.

About Panthera