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Employers

Clinical Trials Coordinator

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Job ID:

58518

Job Type:

Part Time

Category:

Healthcare

Educations:

GCSE
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Posted:

2025-06-16

Location:

Job Views:

57

Salari:

GBP £35,392 - £42,618
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Job Description:

Job information Clinical Trials Coordinator from the Company Cambridge University Hospitals, this latest Clinical Trials Coordinator job vacancy is located in the city Cambridge located in the country United Kingdom . This latest job opening is open to job seekers who have the latest education / graduate GCSE . Job Vacancies in this Healthcare field have been opened and published up to the specified time.

Job Responsibility:

Main area Clinical Trials Coordinator Grade Band 6 Contract 2 years (Fixed Term contract for 2 years) Hours
    Full time Part time Flexible working
37.5 hours per week (Full Time or Part Time/Flexible working hours may be considered) Job ref 180-RD-245295 Employer Cambridge University Hospitals NHS Foundation Trust Employer type NHS Site Addenbrookes Hospital-Division R&D Town Cambridge Salary£35,392 - £42,618 p.a. pro rata Salary period Yearly Closing 17/07/2024 23:59

Job overview

An exciting opportunity has come up to join the Cambridge Clinical Trials Unit (CCTU). The CCTU is a UKCRC Registered Clinical Trials Unit and caters for all investigators of Cambridge University Health Partners (CUHP), and beyond and has responsibility for new and existing clinical trials and clinical research projects on the CCTU portfolio, including Clinical Trials of Investigational Medicinal Products under the EU Directive (CTIMPS).

Main duties of the job

The key job functions of the Clinical Trials Coordinator are:

    To facilitate and co-ordinate the set-up and conduct of clinical trials and/or clinical studies working closely with the chief investigators and their teams

    To have responsibility for setting-up participating sites in multi-centre trials and ensuring that all data and samples are collected following the protocol

    To work in compliance with the International Conference on Harmonisation Good Clinical Practice Guidelines (ICH-GCP), the NHS Research Governance Framework for Health & Social Care and, in the case of a CTIMP, in compliance with the Medicines for Human Use (Clinical Trials) Regulations 2004.

Please see the job description for more detailed duties.

Working for our organisation

Our Trust

Cambridge University Hospitals (CUH) NHS Foundation Trust comprises Addenbrooke's Hospital and the Rosie Hospital in Cambridge. With over 13,000 staff and over 1100 beds the priorities of the Trust focus on a quality service which is all about people - patients, staff and partners. Recognised as providing ‘outstanding' care to our patients and rated ‘Good' overall by the Care Quality Commissioner, is testament to the skill and dedication of the people who work here. CUH's values - Together - Safe, Kind, Excellent - are at the heart of patient care, defining the way all staff work and behave. The Trust provides accessible high-quality healthcare for the local people of Cambridge, together with specialist services, dealing with rare or complex conditions for a regional, national and international population.

CUH is committed to promoting a diverse and inclusive community - a place where we can all be ourselves. We value our differences and fully advocate and support an inclusive working environment where every individual can fulfil their potential. We want to ensure our people are truly representative of all the communities that we serve. We welcome applications for all positions in the organisation irrespective of people's age, disability, ethnicity, race, nationality, gender identity, sex, sexual orientation, religion or belief, marriage and civil partnership status, or pregnancy and maternity status or social economic background.

Detailed job description and main responsibilities

Please see the attached Applicant Information Pack (combined Job Description and Person Specification) for key duties and responsibilities.

Please note:- Internal applicants on permanent contracts can only apply for this post as a secondment and must have the approval of your current line manager before applying.

This vacancy will close at midnight on...

Interviews are due to be held on…

Benefits to you

We offer development opportunities and a wide range of benefits including on-site leisure facilities, shopping concourse, day nurseries and access to a great transport system with easy access to airports and rail travel.

Please note if you would like to discuss the required hours of this role further, you should approach the contact given. In some cases, alternative working hours will be considered.

We welcome applications from the Armed Forces.

Person specification

Qualifications

Essential criteria

    Science graduate or equivalent level of knowledge and experience.

    Recent ICH GCP training.

Desirable criteria

    Evidence of post-graduate training in relevant field, and/or continuous professional development in relevant fields.

Experience

Essential criteria

    Experience of working in a clinical research/ healthcare environment.

    Experience of working in an ICH GCP/EU Clinical Trials Directive environment.

    Experience with databases.

    Previous direct clinical trials and/or project management experience.

Desirable criteria

    Line management experience.

Knowledge

Essential criteria

    Knowledge of the requirements of clinical trials during their life-cycle from set-up to close-out.

    Ability to present data in a clear, simple format.

    Ability to use Microsoft Office to an advanced level.

    Competence in using the internet and email.

    Knowledge of clinical trials regulatory framework.

Desirable criteria

    Clinical trials terminology and essential documentation.

    Study design.

    Knowledge of the clinical trials regulatory framework.

    An understanding of the clinical research approval process in the NHS.

Skills

Essential criteria

    Excellent administrative skills including organising and planning

    Excellent communication skills.

    Excellent attention to detail.

    Helpful, outgoing team worker.

    Excellent interpersonal, professional and motivational skills with the ability to build working relationships with internal and external departmental and Trust colleagues.

    Ability to work under pressure, prioritise and seek input where necessary.

    Ability to work independently with initiative and motivate self and others.

    Ability to maintain confidentiality.

    Ability to negotiate, acting in a tactful and confident manner to achieve the desired results.

Desirable criteria

    Problem solver

    Focused, starter-finisher

    Willing to coach and train others

Additional Requirements

Essential criteria

    The ability to understand and behave at all times, towards patients, visitors and colleagues according to the Trust values of safe, kind, excellent.

    Flexible approach to working and a desire to develop knowledge and career.

    Can demonstrate autonomous working practices in current post.

    Problem solver.

    Focused, starter-finisher.

    Willing to coach and train others.

    Ability to travel to participating sites to conduct on-site visits.

Further details / informal visits contact

Name Ellie Evans-Evans Job title Senior Clinical Research and Education Manager Email address eleanor.evans-evans1@nhs.net Telephone number 01223 256653 Additional information Please feel free to email or call me to discuss this role or arrange visiting the department. Keywords : Cambridge jobs
Closed Date : 2025-07-16
Company Info

Cambridge University Hospitals

Cambridge, United Kingdom

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