Study Coordinator – Preston • Panthera is hiring! Come & join the team! We are looking for an experienced and highly organised Study Coordinator to join our team at our at our Preston Clinical Research Site. This is a key site based role and we are looking for an individual to join the team, taking study ownership, keeping studies on track and making sure the detail is right. You’ll work closely with clinical teams, monitors, vendors and site colleagues to support the smooth delivery of clinical trials! If you have experience working in clinical research and are confident managing study documentation, data and competing priorities, we’d love to hear from you. Salary & Key Benefits: Salary from £27300 to £38,850 25 days’ annual leave plus bank holidays, increasing with length of service Annual Leave Buy and Sell Scheme Life insurance at 3x annual salary Employee healthcare cash plan Employee Assistance Programme Enhanced sickness and family-friendly policies Electric Car Scheme Annual Self-Care Day Key Responsibilities: As a Study Coordinator, you’ll play an important role in the day-to-day management and successful delivery of studies at our York site. Your responsibilities will include: Taking ownership of study trackers, timelines, enrolment and overall study progress Leading day-to-day study coordination and ensuring the site is ready for key study activities, including pre-randomisation Coordinating communication between study teams, vendors, monitors and site colleagues Maintaining accurate and timely study documentation, including the Investigator Site File (ISF), study logs and electronic data capture (EDC) systems Completing accurate data entry and supporting timely query resolution Preparing for and supporting CRA monitoring visits Supporting safety reporting requirements, including Serious Adverse Events (SAEs) Helping ensure studies are delivered in line with protocols, regulatory requirements and site procedures There may occasionally be a requirement to support other local Panthera sites. What we are looking for? You’ll be someone who is organised, detail-focused and comfortable taking responsibility for multiple study activities at once. Previous experience in clinical research or a similar regulated environment Experience coordinating clinical studies and maintaining study documentation Strong data-entry skills with excellent attention to accuracy and deadlines A good understanding of clinical trial documentation and regulatory requirements Strong communication skills and the confidence to work with colleagues, monitors and external partners The ability to prioritise effectively and keep studies moving forward We are an equal opportunity employer and consider all qualified applicants equally without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, veteran status or disability status. AI • Please note, AI may be used in our recruitment process however all CV's are manually viewed by the team.