Trial Monitor

London, ENG, GB, United Kingdom

Job Description

Ref Number


B02-09804

Professional Expertise


Research and Research Support

Department


School of Life & Medical Sciences (B02)

Location


London

Working Pattern


Full time

Salary


43,981-52,586

Contract Type


Fixed-term

Working Type


Hybrid

Available for Secondment


No

Closing Date


06-Jan-2026

About us


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UCL Institute of Clinical Trials and Methodology was established on 1st August 2013 and is formally comprised of two research departments: The MRC Clinical Trials Unit at UCL (MRC CTU) and the Comprehensive Clinical Trials Unit at UCL (CCTU). The Institute also has two further units that are virtual members: The Cancer Research UK & UCL Cancer Trials Centre and the PRIMENT Clinical Trials Unit.



The Faculty brings together expertise in Child Health, Women's and Reproductive Health, Population Health, Global Health, Cardiovascular Science, Clinical Trials and Health Informatics, in a unique grouping that spans the life-course.



The Comprehensive Clinical Trials Unit is a specialist unit set up within the Institute of Clinical Trials and Methodology with a specific remit to design, conduct, analyse and publish clinical trials and other well-designed studies. The CCTU provides clinical, statistical, and trial operations leadership and facilitate the delivery of high quality, regulatory compliant clinical trials of both investigational medicinal products (IMPs) (in compliance with the UK regulations governing the conduct of clinical trials of IMP) and other non-IMP trials and studies.



The CCTU is a registered CTU with the capability to centrally coordinate multi-centre clinical trials (i.e. having overall responsibility for the design, development, recruitment, data management and analysis of trials) with robust systems to ensure conduct and delivery of clinical trials to the highest quality standards.




About the role


------------------


We currently have a full time Clinical Trial Monitor vacancy to work within the unit, which is based in Holborn - London.



We are looking for an individual with good scientific and clinical trial knowledge. The primary role of the post is to conduct clinical trial monitoring activities to ensure the rights, safety and well-being of participants are protected, reported trial data are accurate, and the trial(s) are conducted in compliance with the protocol and applicable regulatory frameworks e.g. GCP.



The post holder will also be expected to provide trial management support to various high-quality clinical trials at the CCTU. This will include monitoring site compliance, data quality and recruitment, and supporting trials through close-out and archiving.



The role is available until August 2027 and involves regular travel to destinations within the UK and Ireland.



The post holder will report to the Head of Clinical Trials Operations.



Interviews will be held in person w/c 19th January 2026 at 90 High Holborn.



A job description and person specification is available at the bottom of the page. Please provide your CV and a cover letter explaining how your skills and experience are applicable to the role.


About you


-------------


An enthusiastic, committed and professional individual.



The successful applicant must possess a degree and/or equivalent experience in clinical trials, as well as recent experience managing and performing on-site monitoring of clinical trials involving Investigational Medicinal Products, a comprehensive understanding of UK Clinical Trials Regulations, the European Directives on Clinical Trials and Good Clinical Practice and the Department of Health's Research Governance Framework.



Other essential qualities required by the role include good communication skills, an ability to work within a multi-disciplinary team, experience of study trial documentation development, excellent attention to detail and organisational skills, and a willingness to travel within the UK and Ireland. Previous experience working in neurology, rheumatology, paediatric and novel First-in-human (FIH) clinical trials would be advantageous.



If you have any queries regarding the vacancy, please contact Anvi Wadke a.wadke@ucl.ac.uk


What we offer


-----------------


As well as the exciting opportunities this role presents we also offer some great benefits some of which are below:


41 Days holiday (including 27 days annual leave 8 bank holiday and 6 closure days) Defined benefit career average revalued earnings pension scheme (CARE) Cycle to work scheme and season ticket loan On-Site nursery On-site gym Enhanced maternity, paternity and adoption pay Employee assistance programme: Staff Support Service Discounted medical insurance

Our commitment to Equality, Diversity and Inclusion


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As London's Global University, we know diversity fosters creativity and innovation, and we want our community to represent the diversity of the world's talent. We are committed to equality of opportunity, to being fair and inclusive, and to being a place where we all belong. We therefore particularly encourage applications from candidates who are likely to be underrepresented in UCL's workforce. These include people from Black, Asian and ethnic minority backgrounds; disabled people; LGBTQI+ people; and for our Grade 9 and 10 roles, women. You can read more about our commitment to Equality, Diversity and Inclusion here : https://www.ucl.ac.uk/equality-diversity-inclusion/

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Job Detail

  • Job Id
    JD4382344
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Full Time
  • Job Location
    London, ENG, GB, United Kingdom
  • Education
    Not mentioned