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Study Coordinator 3

On-site in York·Full-time·Added 1 month ago (last checked 9 Oct)

Overview

Job details

  • £31,500 a year

    Gross, as stated in the ad.

    About £2,180 a month after tax.

  • Full-time

    Per the ad.

Requirements

  • Work on-site in York

    No relocation package mentioned.

Benefits

  • 25 days holiday + bank holidays

    Paid annual leave, per the ad.

  • Cycle to work scheme

    Commuter benefits named in the ad.

Skills

The role

Panthera Biopartners

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.

We put the patient at the heart of everything we do to ensure the best experience and environment for volunteers and participants. Accelerating clinical breakthrough for our customers, our patients, and for future generations.

Study Coordinator 3 - York

A new & exciting opportunity has arisen for a Study Coordinator to join our team at our York Clinical Research Site.

Salary & Benefits Package

  • Salary starting from; £31500
  • 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 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.

    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)
  • Ideal Candidate

  • Highly organised and data driven.
  • Skilled in accurate, timely data entry and query resolution
  • Evidence of experience working in a similar environment.
  • Panthera Biopartners provided the following inclusive hiring information:

    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.

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