Clinical trial administrator Work, Jobs in Wanstead, Gtl (with Salaries)

Research Administrator
Great Ormond Street Hospital for Children —London
- £34,186 - £37,389 a year
- Part-time
- Computer literacy
- Administrative experience
- Organisational skills
8d
Drug Safety Associate II
Corbus Pharmaceuticals Inc —London
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Nursing
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14d
IT Support Specialist
Pharmaron —Hoddesdon
- Azure
- Computer Science
- Windows
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Senior HR Administrator
Fitzrovia Hospital —London
- £30,000 - £35,000 a year
- Full-time
- Hospital
- Microsoft Office
- Human resources
- Annual leave
- Sick pay
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14d
Senior Administration Assistant
The Royal Marsden NHS Foundation Trust —Chelsea
- £31,554 - £33,270 a year
- Full-time
- Administrative experience
- IT
- Time management
8h
Senior Microsoft 365 Platform Engineer
Pharmaron —Hoddesdon
- Microsoft Access
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- Bachelor's degree

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clinical trial administrator jobs near wanstead, gtl

Research Administrator

Great Ormond Street Hospital for Children -
London

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Job details

Part-time
£34,186 - £37,389 a year
8 days ago

Benefits

UK visa sponsorship

Qualifications

Computer literacy
Filing
Administrative experience
Organisational skills
IT
Computer skills
NVQ
Communication skills

Full job description

Main area

Neuromuscular

Grade

Band 4

Contract

12 months (Fixed Term)

Hours

Part time - 15 hours per week

Job ref

271-R&I-7915355-A

Site

UCL Great Ormond Street Institute for Child Health

Town

London

Salary

£34,186 - £37,389 pro rata per annum inclusive

Salary period

Yearly

Closing

28/07/2026 23:59

Job overview

An exciting opportunity has arisen for a Research Administrator to join our dynamic Neuromuscular research team working within the NIHR Clinical Research Facility and throughout Great Ormond Street Hospital for Children.

The Dubowitz Neuromuscular Centre at Great Ormond Street Hospital and UCL Great Ormond Street Institute of Child Health, follows a large number of children affected by a variety of neuromuscular disorders and is a leading international centre for the research, management and therapy of childhood neuromuscular disorders. The Centre is the largest paediatric neuromuscular centre in UK and has a strong research interest in the causes and treatment of muscular dystrophies and other neuromuscular disorders in children. The Centre is part of the MRC Neuromuscular Translational research centre at UCL in collaboration with the adult neurologist team of the Institute of Neurology at Queen Square. Further information on the MRC centre can be found at www.cnmd.ac.uk.

You will be joining an enthusiastic and motivated multidisciplinary team working within a centre of excellence in central London. GOSH offers flexible working, help with childcare and travel, excellent training and development opportunities and assistance with finding somewhere to live.

Main duties of the job

The Research Administrator will provide support in a clinical and academic research environment for the delivery of clinical research within the GOSH/UCL neuromuscular team and the Clinical Research Facility (CRF),

The post holder will be responsible for providing administrative support to both the clinical and non-clinical neuromuscular delivery teams in organising, attending, and documenting meetings or training events relevant to the start-up, conduct or closure of studies and projects.

The post holder will act as a point of contact for other day to day administrative tasks such as coordination of PI calendars, meeting organisation and supporting the team in the hosting of events and workshops for members of wider neuromuscular networks. The post holder will at times also be responsible for capturing complex clinical data from medical records and research documentation and entering data into electronic systems for non-commercial, investigator led studies or the NorthStar/SMA REACH UK projects ensuring that data is recorded accurately and submitted in a timely manner. This role will involve effective communication with research and clinical teams within the Trust and external stakeholders.

The post holder might be involved with the coordination of study start up activities and the preparation and maintenance of local study documentation relating to: clinical study timelines, recruitment plans and strategy, informed consent forms and amendments.

Working for our organisation

We are committed to recruiting the best person for the job through a fair, open and consistent process that is free from bias and discrimination.

We are working towards becoming an anti-racist organisation. This means creating a workplace where every colleague feels seen, heard and valued, and where racism in any form has no place. Our anti-racism commitment is backed by action through our Anti-Racism Statement and action plan, developed in collaboration with our REACH staff network.

We actively challenge discrimination, dismantle barriers and embed equity across all aspects of our workforce, including recruitment, progression and development. All applicants will receive equal consideration regardless of race, ethnicity, nationality, religion or belief, sexual orientation, gender identity, age, disability, health condition or employment history.

We particularly welcome applications from ethnically diverse communities, people with disabilities or long-term health conditions, and LGBTQ+ community members. We are proud to be a Disability Confident Employer, a member of the Business Disability Forum, and a Stonewall Diversity Champion.

Our staff networks, including REACH, PRIDE, ENABLED and Women’s Networks, are active and executive supported. These employee-led networks play a vital role in shaping an inclusive culture at GOSH and are open to all colleagues.

Together, we are building a culture where inclusion is not optional - it is essential.

Detailed job description and main responsibilities

The full job description provides an overview of the key tasks and responsibilities of the role, and the person specification outlines the qualifications, skills, experience and knowledge required. For both documents please view the attachment/s below.

Person specification

GOSH Culture and Values

Essential criteria

Gosh Values
Experience of working as part of a diverse team.
Experience of contributing to an inclusive workplace culture.

Academic/Professional qualification/Training

Essential criteria

Qualified to ‘A’ Level/NVQ Level 3 standard or equivalent
Knowledge of health information management acquired through a relevant specialist qualification or equivalent experience of information handling and analysis gained in a work environment

Desirable criteria

Educated to degree level in a relevant discipline (i.e. science, health, health management, social science)

Experience/Knowledge

Essential criteria

Experience of working on multiple parallel tasks to strict and often tight deadlines
Experience of managing information systems and developing databases and spreadsheets
Experience of analysing complex information from databases
Relevant secretarial/administrative experience (ideally in a health care setting)
Knowledge of the Data Protection Act
Experience of setting up and managing filing systems

Desirable criteria

Knowledge and understanding of the Department of Health’s Research Governance Framework
Experience of working in a clinical trial environment in either a pharmaceutical company, NHS Trust or a university

Skills/Abilities

Essential criteria

Computer literate with good IT skills including the upkeep of databases
Excellent verbal and written communication skills, with the ability to interact effectively with staff at all levels
Able to handle sensitive and/or confidential information
Able to transcribe data in a timely and accurate manner with excellent attention to detail
Able to work calmly under pressure in order to manage an unpredictable workload and perform to tight deadlines
Ability to extract, compile and interrogate data
Good organisational skills including the ability to prioritise workload
Ability to work autonomously and use own initiative with minimal day to day supervision

Please be advised that:

The recruitment process for all admin and clerical roles at Bands 2-4 will be a two stage recruitment process whereby shortlisted candidates will undertake an online literacy, numeracy, ICT and typing test. Only those candidates who pass the competency test will proceed to a formal interview.

The closing date given is a guide only. There may be some occasions where we have to close a vacancy once sufficient applications have been received. It is therefore advisable that you submit your application as early as possible to avoid disappointment.

Only those candidates who clearly demonstrate how they meet the person specification criteria for this post will be shortlisted. Please note that where high volumes of applicants have been received, additional criteria may on occasion be used to determine the final shortlist.

Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website .

We are an accredited Living Wage Employer.

Applicant requirements

This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service.

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clinical trial administrator jobs in wanstead, gtl

Research Administrator

Drug Safety Associate II

IT Support Specialist

Senior HR Administrator

Senior Administration Assistant

Senior Microsoft 365 Platform Engineer

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Job overview

Main duties of the job

Working for our organisation

Detailed job description and main responsibilities

Person specification

GOSH Culture and Values

Essential criteria

Academic/Professional qualification/Training

Essential criteria

Desirable criteria

Experience/Knowledge

Essential criteria

Desirable criteria

Skills/Abilities

Essential criteria

Please be advised that:

Applicant requirements

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