At a Glance
- Tasks: Manage clinical trial data and ensure compliance with regulatory standards.
- Company: Join a leading clinical research team at our York site.
- Benefits: Competitive salary, generous leave, healthcare cash plan, and more.
- Other info: Dynamic role with opportunities for growth across multiple sites.
- Why this job: Make a real difference in clinical research while developing your skills.
- Qualifications: Strong organisational skills and attention to detail required.
The predicted salary is between 27300 - 32550 £ per year.
An exciting opportunity has arisen for a Patient Study Coordinator 2 to join our team at our York Clinical Research Site.
Salary & Benefits Package:
- Salary starting from: £27300 - £32550
- 25 days annual leave plus bank holidays increasing with length of service
- Annual Leave Buy and Sell Scheme
- Life insurance - 3x annual salary
- Employee healthcare cash plan
- Employee Assistant Programme
- Enhanced sickness and family friendly policies
- Annual Self Care Day
- Cycle to Work Scheme
- EV Scheme
Job Summary:
The Patient Study Coordinator 2 plays a key role in managing clinical trial data and supporting site compliance with regulatory and protocol standards. The role involves detailed data entry, documentation tracking, CRA visit preparation, and ensuring clinical and administrative readiness across all trial activities. There may be a requirement to work across local Panthera sites as required from time to time.
Key Responsibilities:
- Oversee study trackers, timelines, enrolment, and overall study progress
- Lead day-to-day site management and ensure study readiness (including Pre-Rand activities)
- Coordinate communication between study teams, vendors, monitors, and site staff
- Ensure accurate documentation, data entry, and regulatory compliance (ISF, logs, EDC)
- Support monitoring activities, CRA visits, and safety reporting (including SAEs)
We think you need these skills to ace Study Coordinator 2
Data Entry
Documentation Tracking
Regulatory Compliance
Clinical Trial Management
Communication Skills
Site Management
Study Coordination
