At a Glance
- Tasks: Manage clinical trial data and ensure site compliance with regulations.
- Company: Panthera Biopartners, a leader in clinical research based in York.
- Benefits: Competitive salary, flexible hours, and opportunities for professional growth.
- Other info: Collaborative environment with potential for cross-site work.
- Why this job: Play a crucial role in advancing medical research and improving patient outcomes.
- Qualifications: Experience in clinical trials and strong organisational skills.
The predicted salary is between 30000 - 40000 £ per year.
Panthera Biopartners in York is seeking a Patient Study Coordinator 2 to help manage clinical trial data and support site compliance with regulatory and protocol standards. The role involves detailed data entry, documentation tracking, CRA visit preparation, and ensuring readiness across all trial activities. There may be occasional cross-site work across Panthera locations. You will oversee trackers, enrolment, and study progress, coordinate communication among study teams and monitors.
Clinical Study Coordinator II - Data & Site Readiness employer: Panthera Biopartners
At Panthera Biopartners, we pride ourselves on fostering a collaborative and innovative work culture that prioritises the well-being of both our employees and the patients we serve. Located in York, our team enjoys a competitive salary, generous annual leave, and ample opportunities for professional growth in the dynamic field of clinical research. Join us to be part of a mission-driven organisation where your contributions truly make a difference.
