Skip to main content
Post your CV and find your next job on Indeed!

Clinical Trials Assistant jobs in London

Sort by: -

People also searched:

trainee

Job Post Details

Study Coordinator 3 - job post

Panthera Biopartners
4.0 out of 5 stars
London EN3 4GS
From £34,650 a year - Permanent, Full-time

Job details

Pay

  • From £34,650 a year

Job type

  • Permanent
  • Full-time

Location

London EN3 4GS

Benefits

Pulled from the full job description

  • Annual leave
  • Life insurance
  • Cycle to work scheme

Full job description

Patient Study Coordinator 3 - Enfield

An exciting opportunity has arisen for a Patient Study Coordinator 3 to join our team at our Enfield 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.

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.

Salary & Benefits Package

  • Salary starting from; £34650
  • 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 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.
  • Previous experience in the healthcare sector is desirable but not essential.

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.

INDHP

Job Types: Full-time, Permanent

Pay: From £34,650.00 per year

Ability to commute/relocate:

  • London EN3 4GS: reliably commute or plan to relocate before starting work (preferred)

Application question(s):

  • What is your current notice period?
  • What are your salary expectations?
  • Do you require sponsorship either now or in the future?

Work authorisation:

  • United Kingdom (preferred)

Work Location: In person

Let Employers Find YouUpload Your Resume