Clinical research assistant Work, Jobs in Radlett, Hrt (with Salaries)

Clinical Trial Assistant – Observational Studies
Oracle —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Life insurance
Research Assistant
University College London Hospitals NHS Foundation Trust —London
- £38,488 - £46,852 a year
- Full-time
- Organisational skills
- Communication skills
5d
Research Assistant
University College London —London
- £21,139.92 - £41,833.00 a year
- Part-time
- Master's degree
- Annual leave
- Employee assistance programme
13d
Research Assistant (Maini Lab)
University College London —London
- £36,433 - £41,833 a year
- Full-time
- Communication skills
- Annual leave
- Employee assistance programme
5h
Research Assistant in Brain Vascular Epigenomics – UK Dementia Research Institute
Imperial College London —White City
- £43,863 - £47,223 a year
- Full-time
- C++
- University
- Linux
2d
Research Fellow in Brain Vascular Biology and Brain Cancer Biology
University College London —London
- £43,374 - £51,860 a year
- Full-time
- Doctoral degree
- English
- University
- Annual leave
- Employee assistance programme
Research Nurse in Infection and Sexual Health
University College London —London
- £43,981 - £52,586 a year
- Full-time
- Communication skills
- Teaching
- Time management
- Annual leave
- Employee assistance programme
5d
Research Assistant - Bank
hVIVO Services Limited —London
- Weekend availability
- Laboratory experience
- Communication skills
Research Fellow in Eating Disorders Epidemiology
University College London —London
- £38,607 - £52,586 a year
- Part-time
- Doctoral degree
- Analysis skills
- Communication skills
- Annual leave
- Employee assistance programme
1d
UKDTN Coordinating Centre Administrative Assistant
University College London —London
- £36,433 - £41,833 a year
- Full-time
- Hybrid work
- Administrative experience
- Contracts
- Communication skills
- Annual leave
- Employee assistance programme
12d
Research Fellow
University College London —London
- £45,103 - £49,943 a year
- Full-time
- Doctoral degree
- Master's degree
- Administrative experience
- Annual leave
- Employee assistance programme
1d
Research Associate in ISAP study
Imperial College London —Hammersmith
- £49,017 - £57,472 a year
- Full-time
1d
Research Nurse
University College London Hospitals NHS Foundation Trust —London
- £47,951 - £56,863 a year
- Full-time
9d
Clinical Research Fellow Hepatology Medicine
Chelsea and Westminster Hospital NHS Foundation Trust —London
- £49,909 - £61,825 a year
- Full-time
5d
Research Associate
Imperial College London —White City
- £49,017 - £57,472 a year
- Full-time
- Doctoral degree
- Engineering
- Data analysis skills
13d
Clinical Research Nurse
Central and North West London NHS Foundation Trust —London
- £47,951 - £56,863 a year
- Full-time
- Travel
5d
Research Associate in Osteoarthritis Biostatistics
Imperial College London —Hammersmith
- £49,017 - £57,472 a year
- Full-time
- Hybrid work
- Doctoral degree
- Computer skills
- Communication skills
Senior Clinical Scientist (Medical Physicist) –Clinical Trials Lead
University College London Hospitals NHS Foundation Trust —London
- £66,274 - £73,496 a year
- Full-time
6d
Senior Clinical Research Manager
University College London —London
- £68,284 - £76,244 a year
- Full-time
- Master's degree
- Leadership
- Negotiation
- Annual leave
- Employee assistance programme
2d

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clinical research assistant jobs near radlett, hrt

Clinical Trial Assistant – Observational Studies

Oracle -
London

Apply Now

Job details

Full-time

Benefits

Life insurance

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Oracle
Clinical research
Customer service
English
Administrative experience
Bachelor's degree
Organisational skills

Full job description

Oracle Life Sciences empowers pharmaceutical, biotechnology, medical device companies, and clinical research organizations to bring therapies to market faster and more efficiently. We are helping organizations accelerate innovation and improve health outcomes for patients worldwide.

With ongoing and ground-breaking developments in Oncology and Rare Disease, an increased focus on more scientific, targeted medicine and continuous integration of technology into development and delivery of medicine, there has never been a more exciting time to join us!

We are currently seeking a highly organized and detail-oriented Clinical Trial Assistant (CTA) to provide essential administrative support to our clinical project teams.

This role is heavily focused on clinical documentation, Trial Master File (TMF) management, and coordination activities supporting observational research programs.

Working Environment

Hybrid working model: 1–2 days per week in the London office.

Please note: Prior experience supporting clinical interventional or observational studies is a mandatory requirement.

Only Oracle brings together the data, infrastructure, applications, and expertise to power everything from industry innovations to life-saving care. And with AI embedded across our products and services, we help customers turn that promise into a better future for all. Discover your potential at a company leading the way in AI and cloud solutions that impact billions of lives.

True innovation starts when everyone is empowered to contribute. That’s why we’re committed to growing a workforce that promotes opportunities for all with competitive benefits that support our people with flexible medical, life insurance, and retirement options. We also encourage employees to give back to their communities through our volunteer programs.

We’re committed to including people with disabilities at all stages of the employment process. If you require accessibility assistance or accommodation for a disability at any point, let us know by emailing [email protected] or by calling 1-888-404-2494 in the United States.

Oracle is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans’ status, or any other characteristic protected by law. Oracle will consider for employment qualified applicants with arrest and conviction records pursuant to applicable law.

What you will do

Supporting Trial Master File (TMF) creation and maintenance.
Managing the set-up, organization, processing, and archiving of all clinical trial documents throughout all project phases.
Assisting in the preparation and delivery of Investigator Site Files (ISF).
Ensuring compliance and quality standards for documentation and participating in file audits.

Required Experience

Bachelor's degree (preferably in Life Sciences, Healthcare Administration, or a related field) or equivalent relevant experience.
Mandatory: Minimum 2 years of experience supporting interventional or observational studies in a Clinical Trial Assistant, Study Coordinator, Site Coordinator, or similar administrative clinical research role.
Demonstrated experience with clinical trial documentation management, including Trial Master Files (TMF) and Investigator Site Files (ISF).
Strong administrative, organizational, and multitasking skills with exceptional attention to detail.
Experience coordinating study documentation, tracking deliverables, and supporting audit readiness activities.
Outstanding spoken and written English proficiency (minimum C1 level). Additional languages are considered a strong asset.
Proficiency in Microsoft Word, Excel, PowerPoint, and document management systems.
Excellent interpersonal and customer service skills with the ability to work effectively across cross-functional teams.
Proactive, dependable, and committed to delivering high-quality administrative support in a fast-paced environment.

What you will do

Supporting Trial Master File (TMF) creation and maintenance.
Managing the set-up, organization, processing, and archiving of all clinical trial documents throughout all project phases.
Assisting in the preparation and delivery of Investigator Site Files (ISF).
Ensuring compliance and quality standards for documentation and participating in file audits.

Required Experience

Bachelor's degree (preferably in Life Sciences, Healthcare Administration, or a related field) or equivalent relevant experience.
Mandatory: Minimum 2 years of experience supporting interventional or observational studies in a Clinical Trial Assistant, Study Coordinator, Site Coordinator, or similar administrative clinical research role.
Demonstrated experience with clinical trial documentation management, including Trial Master Files (TMF) and Investigator Site Files (ISF).
Strong administrative, organizational, and multitasking skills with exceptional attention to detail.
Experience coordinating study documentation, tracking deliverables, and supporting audit readiness activities.
Outstanding spoken and written English proficiency (minimum C1 level). Additional languages are considered a strong asset.
Proficiency in Microsoft Word, Excel, PowerPoint, and document management systems.
Excellent interpersonal and customer service skills with the ability to work effectively across cross-functional teams.
Proactive, dependable, and committed to delivering high-quality administrative support in a fast-paced environment.

Apply Now

Refine Your Search

clinical research assistant jobs in radlett, hrt

Clinical Trial Assistant – Observational Studies

Research Assistant

Research Assistant

Research Assistant (Maini Lab)

Research Assistant in Brain Vascular Epigenomics – UK Dementia Research Institute

Research Fellow in Brain Vascular Biology and Brain Cancer Biology

Research Nurse in Infection and Sexual Health

Research Assistant - Bank

Research Fellow in Eating Disorders Epidemiology

UKDTN Coordinating Centre Administrative Assistant

Research Fellow

Research Associate in ISAP study

Research Nurse

Clinical Research Fellow Hepatology Medicine

Research Associate

Clinical Research Nurse

Research Associate in Osteoarthritis Biostatistics

Senior Clinical Scientist (Medical Physicist) –Clinical Trials Lead

Senior Clinical Research Manager

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