Clinical audit Work, Jobs in London (with Salaries)

Clinical Trial Assistant – Observational Studies
Oracle —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Life insurance
Part Time Clinical Data Coordinator
HCA Healthcare UK —London
- Up to £13,600 a year
- Part-time
- Employee discount
1d
Clinical Compliance Lead
Communitas Clinics —South East London
- From £45,000 a year
- Full-time
- Hybrid work
- Anatomy knowledge
- Travel
- Patient care
Quick apply
Clinical Support Specialist - 12 month FTC, Full-Time
hVIVO Services Limited —London
- Overtime
- Customer service
- Administrative experience
- IT
- Annual leave
- Employee assistance programme
14d
Clinical Ward Fellow
Cleveland Clinic London —London
- Full-time
- Management
- Supervising experience
- Leadership
Clinical Data Coordinator
HCA Healthcare UK —London
- Up to £34,000 a year
- Full-time
- Employee discount
1d
Quality and Regulatory Officer
Hertility —London
- £35,000 - £40,000 a year
- Full-time
- Remote
- Engineering
- Analysis skills
- Travel
- Annual leave
- Employee discount
11d
Clinical Embryologist
CRGH —London
- Doctoral degree
- Laboratory experience
- English
- Annual leave
- Employee discount
Quick apply
8d
Clinical Governance Clinician
Acacium Group —London
- £48,000 a year
- Full-time
- Remote
- Presentation skills
- Communication skills
- Employee assistance programme
Quick apply
1d
Clinical Research Nurse
Perceptive —London
- Full-time
- Computer literacy
- Communication skills
- Nursing
- Free parking
Clinical Support Specialist - Bank, Full-Time
hVIVO Services Limited —London
- £13.50 an hour
- Overtime
- Customer service
- Administrative experience
- IT
14d
Drug Safety Associate II
Corbus Pharmaceuticals Inc —London
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Nursing
Quick apply
Clinical Specialist Nuclear Medicine Technologist
HCA Healthcare UK —London
- Full-time
- Bachelor's degree
- Patient care
- Employee discount
Urological Clinical Fellow
Cleveland Clinic London —London
- Full-time
- Doctoral degree
- Master's degree
- Bachelor's degree
11d
Clinical Trainer
Capita —London
- £43,000 a year
- Full-time
- Presentation skills
- Continuous improvement
- Travel
- Employee discount
Digital Advanced Clinical Practitioner
Doctor Care Anywhere —London
- £60,169 a year
- Part-time
- Remote
- Master's degree
- IT
- Communication skills
- Annual leave
Quick apply
Auditor - PIP (Functional Specialist - Quality)
Capita —London
- £41,500 a year
- Full-time
- Remote
- Continuous improvement
- Employee discount
12d
Clinical Data Manager II/Senior Clinical Data Manager
Precision Medicine Group —London
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Associate Director, Clinical Data Management
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Bachelor's degree
- Travel
- In-person
Quality Assurance Manager - Cell & Gene Therapy Service
Great Ormond Street Hospital for Children —London
- £66,274 - £73,496 a year
- Full-time
- Microsoft Powerpoint
- Supervising experience
- Bachelor's degree
2d

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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 audit jobs in london

Clinical Trial Assistant – Observational Studies

Part Time Clinical Data Coordinator

Clinical Compliance Lead

Clinical Support Specialist - 12 month FTC, Full-Time

Clinical Ward Fellow

Clinical Data Coordinator

Quality and Regulatory Officer

Clinical Embryologist

Clinical Governance Clinician

Clinical Research Nurse

Clinical Support Specialist - Bank, Full-Time

Drug Safety Associate II

Clinical Specialist Nuclear Medicine Technologist

Urological Clinical Fellow

Clinical Trainer

Digital Advanced Clinical Practitioner

Auditor - PIP (Functional Specialist - Quality)

Clinical Data Manager II/Senior Clinical Data Manager

Associate Director, Clinical Data Management

Quality Assurance Manager - Cell & Gene Therapy Service

I want to receive the latest job alerts for clinical audit in london

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