Clinical Study Coordinator II - Data & Site Ops

Clinical Study Coordinator II - Data & Site Ops

Full-Time 30000 - 40000 Β£ / year (est.) No working from home possible
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At a Glance

  • Tasks: Manage trial data and ensure smooth operations for clinical studies.
  • Company: Join Panthera Biopartners, a leader in clinical research.
  • Benefits: Competitive salary, supportive team environment, and career development opportunities.
  • Other info: Dynamic role with opportunities to collaborate with diverse teams.
  • Why this job: Make a difference in patient safety and contribute to groundbreaking research.
  • Qualifications: Experience in clinical trials and strong organisational skills.

The predicted salary is between 30000 - 40000 Β£ per year.

Panthera Biopartners in York is seeking a Patient Study Coordinator 2 to join our clinical research site.

You will manage trial data, track documentation, and support regulatory and protocol compliance across studies.

The role involves data entry, site readiness, CRA visit prep, and collaboration with study teams, vendors, monitors, and site staff to ensure smooth trial operations and patient safety.

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Clinical Study Coordinator II - Data & Site Ops 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.

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Contact Details:

Panthera Biopartners Recruitment Team

We think you need these skills to ace Clinical Study Coordinator II - Data & Site Ops

Data Management
Documentation Tracking
Regulatory Compliance
Protocol Compliance
Data Entry
Site Readiness
CRA Visit Preparation