Y-Axis Jobs Logo
Send us feedback
telephone  +91 7670 800 001
Log in Sign up Try Premium
Quality Assurance Officer at Walker Cole International
London, Gloucestershire - England, United Kingdom -
Full Time

Start Date

Immediate

Expiry Date

17 Dec, 26

Salary

30000.0

Posted On

18 Sep, 26

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Pharmaceutical Manufacturing

Description

Full job description

Clinical Trials Assistant

Central London

Full-time, Permanent, Site Based Only

£30-£35,000 per annum


About us

Our client is a highly respected private ophthalmic clinic in London, led by a renowned consultant specialist known for providing exceptional care for patients from the UK and abroad. The clinic combines advanced clinical care with an active clinical trials and research programme covering a range of retinal and ophthalmic conditions.


About the role

This is a varied, hands-on developmental role spanning clinical trial administration, participant coordination, research data management, clinical imaging, sample processing and research support. You will work alongside the Lead Clinical Trials Coordinator, Clinical Trials Coordinators and the wider research team to support the delivery of multiple industry-sponsored and clinic-initiated studies.

This is an Assistant-level, developmental position - extensive previous clinical trials experience is not essential. Structured training will be provided across Good Clinical Practice, ophthalmic imaging, sample handling and Electronic Data Capture systems, with genuine opportunities to take on greater responsibility as your competency develops.


What you'll be doing

  • Supporting the day-to-day organisation and administration of clinical trials, including maintaining accurate study records, trackers and documentation
  • Contacting and coordinating study participants, welcoming and assisting them during their appointments
  • Supporting recruitment and screening activity, including maintaining recruitment trackers
  • Learning to carry out protocol-required ophthalmic imaging and diagnostic testing once appropriately trained and signed off as competent
  • Supporting the collection, preparation, processing and shipment of biological samples
  • Entering and checking study data accurately in Electronic Data Capture systems within agreed timelines
  • Supporting sponsor, CRO and monitor visits, including preparing documentation and locating records
  • Helping collate information for research presentations, reports and academic publications
  • Working in accordance with Good Clinical Practice and maintaining participant confidentiality at all times

What we're looking for

Essential:

  • Excellent organisational skills and a high degree of accuracy and attention to detail
  • The ability to manage multiple tasks, prioritise effectively and work to strict deadlines
  • Confidence using computers, electronic systems and the ability to work with large databases
  • Good written and verbal communication skills
  • A calm, professional and compassionate approach when working with participants and colleagues
  • Reliability, discretion and a proactive approach to work
  • Flexibility regarding duties, shifts and working hours

Desirable:

  • Previous experience within clinical research, clinical trials or a healthcare environment
  • Previous patient-facing experience
  • Experience in ophthalmology or optometry
  • Familiarity with Good Clinical Practice or Electronic Data Capture systems


Working hours

This is a full-time role working 40 hours per week on a shift basis, with typical shifts of 08:00-17:00, 09:00-18:00 or 10:00-19:00. As clinical trials are time-sensitive, some flexibility will be required, including occasional earlier starts, later finishes or weekend work to support protocol-defined visits, treatments or monitoring activity.


If you're organised, detail-focused and looking to build a career in clinical research within a technology-rich ophthalmic clinic, we'd love to hear from you.


This post is subject to the Rehabilitation of Offenders Act 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.


BSR Health are a Specialist Healthcare Agency. If you are interested in working with us, or have any other questions about this role, please don't hesitate to get in touch.
Responsibilities

Full job description

Clinical Trials Assistant

Central London

Full-time, Permanent, Site Based Only

£30-£35,000 per annum


About us

Our client is a highly respected private ophthalmic clinic in London, led by a renowned consultant specialist known for providing exceptional care for patients from the UK and abroad. The clinic combines advanced clinical care with an active clinical trials and research programme covering a range of retinal and ophthalmic conditions.


About the role

This is a varied, hands-on developmental role spanning clinical trial administration, participant coordination, research data management, clinical imaging, sample processing and research support. You will work alongside the Lead Clinical Trials Coordinator, Clinical Trials Coordinators and the wider research team to support the delivery of multiple industry-sponsored and clinic-initiated studies.

This is an Assistant-level, developmental position - extensive previous clinical trials experience is not essential. Structured training will be provided across Good Clinical Practice, ophthalmic imaging, sample handling and Electronic Data Capture systems, with genuine opportunities to take on greater responsibility as your competency develops.


What you'll be doing

  • Supporting the day-to-day organisation and administration of clinical trials, including maintaining accurate study records, trackers and documentation
  • Contacting and coordinating study participants, welcoming and assisting them during their appointments
  • Supporting recruitment and screening activity, including maintaining recruitment trackers
  • Learning to carry out protocol-required ophthalmic imaging and diagnostic testing once appropriately trained and signed off as competent
  • Supporting the collection, preparation, processing and shipment of biological samples
  • Entering and checking study data accurately in Electronic Data Capture systems within agreed timelines
  • Supporting sponsor, CRO and monitor visits, including preparing documentation and locating records
  • Helping collate information for research presentations, reports and academic publications
  • Working in accordance with Good Clinical Practice and maintaining participant confidentiality at all times

What we're looking for

Essential:

  • Excellent organisational skills and a high degree of accuracy and attention to detail
  • The ability to manage multiple tasks, prioritise effectively and work to strict deadlines
  • Confidence using computers, electronic systems and the ability to work with large databases
  • Good written and verbal communication skills
  • A calm, professional and compassionate approach when working with participants and colleagues
  • Reliability, discretion and a proactive approach to work
  • Flexibility regarding duties, shifts and working hours

Desirable:

  • Previous experience within clinical research, clinical trials or a healthcare environment
  • Previous patient-facing experience
  • Experience in ophthalmology or optometry
  • Familiarity with Good Clinical Practice or Electronic Data Capture systems


Working hours

This is a full-time role working 40 hours per week on a shift basis, with typical shifts of 08:00-17:00, 09:00-18:00 or 10:00-19:00. As clinical trials are time-sensitive, some flexibility will be required, including occasional earlier starts, later finishes or weekend work to support protocol-defined visits, treatments or monitoring activity.


If you're organised, detail-focused and looking to build a career in clinical research within a technology-rich ophthalmic clinic, we'd love to hear from you.


This post is subject to the Rehabilitation of Offenders Act 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.


BSR Health are a Specialist Healthcare Agency. If you are interested in working with us, or have any other questions about this role, please don't hesitate to get in touch.