Milton Keynes, England, England £22k – £23k / yr Full Time 🇬🇧 United Kingdom Posted: 2026-07-04

Full Job Description

Key Responsibilities

Study Coordinator responsibilities will include but are not limited to:

To participate in advertising for and recruitment of volunteers suitable for clinical studies.
To screen the volunteers against the inclusion and exclusion criteria.
To obtain clinical histories and samples following enrolment.
To carry out and/or assist with clinical procedures within studies including: phlebotomy, blood laboratory processing and transportation.
To instruct participants on study procedures.
To collect and record clinical data from patients by developing and updating databases.
To maintain accurate documentation of study events in source notes.
To help with participant care while they are in clinical studies and liaise with study physicians as appropriate.
To provide research participants with a point of contact for queries, questions or support.
To help identify, record and report any adverse events.
To contribute to monitoring recruitment progress to ensure compliance with and adherence to the project plan and to identify, evaluate and rectify problems.

Skills and Experience Required:

Job Types: Full-time, Permanent

Salary: £21,600.00-£23,000.00 per year

Benefits:

Schedule:

Supplemental pay types:

Ability to commute/relocate:

Milton Keynes, MK15 0DU: reliably commute or plan to relocate before starting work (required)

Work Location: In person

Application deadline: 30/06/2023
Reference ID: BIOLUMINUX-HSW-2023
Expected start date: 30/06/2023

Company Bioluminux Clinical Research

Location Milton Keynes, England, England

Salary £22k – £23k / yr

Job Type Full Time

Posted 2026-07-04

Deadline 2026-09-04

Country 🇬🇧 United Kingdom

Health Care Support Worker