Clinical Trial Manager (Maternity Cover)

🔒 Confidential Employer
Posted 7 May 2026
LOCATION
London
TYPE
Contract
LEVEL
Mid-Senior level
SALARY
£52,586 / year
CATEGORY
Healthcare
This employer holds a UK Home Office sponsor license — sponsorship for this specific role is at the employer’s discretion

SKILLS

Clinical trial management UK Clinical Trials Regulations Good Clinical Practice (GCP) Investigational Medicinal Products (IMP) Study documentation development Communication skills Attention to detail Organisational skills

FULL DESCRIPTION

Clinical Trial Manager (Maternity Cover)

[Employer hidden — sign up to reveal] - Comprehensive Clinical Trials Unit (CCTU)

Location: London, Hybrid | Salary: £43,981 to £52,586 | Hours: Full Time | Contract Type: Fixed-Term/Contract

Placed On: 5th May 2026 | Closes: 19th May 2026 | Job Ref: B02-10510

About us

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.

About the role

We currently have full time Trial Manager vacancy to work within the unit, which is based in Holborn, London. We are looking for individual with good scientific and clinical trial acknowledge. The primary role of the post holder is to set up and support high quality clinical trial at the [Employer hidden — sign up to reveal].

The role is fixed term maternity cover available until August 2027

The post holder will report to the Clinical Project Manager.

Interviews will be held in person on Thursday 11th June at 90 High Holborn, London.

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 in the coordination 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.

We are looking for someone with good scientific and clinical trial acknowledge. An ideal candidate would possess on-site monitoring experience, 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/or internationally. Previously experience working in neurology, rheumatology and paediatric trials would be advantageous.

An experience of Line Management would be advantageous, however is not essential.

If you have any queries regarding the vacancy please contact [Employer hidden — sign up to reveal]

Customer advert reference: B02-10510

Sign up free — access 45,000+ UK sponsor-licensed jobs