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Panthera Biopartners

Study Coordinator 3

Sheffield
£31.5k/yr
Posted about 17 hours ago
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Study Coordinator 3 - Sheffield

An exciting opportunity has arisen for a Study Coordinator 3 to join our team at our Sheffield Clinical Research Site.

Panthera is an independent Site Management Organisation helping pharmaceutical and contract research organisations find the right patient, for the right trial, at the right time. The Panthera team is run by a world-class team of experts with more than a hundred years of clinical research experience.

Salary & Benefits Package

  • Salary starting from; £31,500
  • 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
  • Enhanced Pension Scheme
  • Annual Self Care Day
  • Cycle to Work Scheme
  • EV Scheme

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Job Summary

The Patient Study Coordinator 3 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.

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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)
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Skills

Clinical Trial Management
Data Entry
Regulatory Compliance
Documentation Tracking
CRA Visit Preparation
Study Tracker Management
Site Management
Safety Reporting
SAE Reporting
EDC
ISF Management
Clinical Research
Vendor Coordination
Protocol Standards

Location

Sheffield, England, United Kingdom

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