Clinical data manager Work, Jobs in Loughton Roding, Ess (with Salaries)

Clinical Data Manager
Cancer Research UK —London
- £39,000 - £44,000 a year
- Full-time
- Remote
- Nursing
- Organisational skills
- Communication skills
1d
Quality Director
Aiyara Partners —Chelmsford
- £100,000 - £110,000 a year
- Full-time
- Management
- Continuous improvement
- Travel
Quick apply
8d
Project Coordinator, Data Monitoring - Entry Level
Medpace, Inc. —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Bachelor's degree
- Annual leave
- Work from home
Quality and Locations Compliance Officer
Communitas Clinics —Croydon
- £35,000 a year
- Full-time
- Hybrid work
- Microsoft Office
- Administrative experience
- Continuous improvement
Quick apply
Clinical Trial Study Manager (1 Year FTC)
Roche —Welwyn
- Bachelor's degree
3d
Head of Clinical Operations
Dispensed —London
- £60,000 - £90,000 a year
- Full-time
- Hybrid work
- Management
- Travel
- Recruiting
Quick apply
9d
eClinical Coordinator (London, Entry Level)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Software troubleshooting
- English
- Annual leave
- Work from home
Junior Project Manager
M3EU —London
- Full-time
- Remote
- Writing skills
- Project management
- Bachelor's degree
- Annual leave
- Employee discount
Quick apply
10d
Clinical Coding Specialist Health Group Lead (Remote/Home Working available, 20% R&R and 5% Fringe)
The Princess Alexandra Hospital NHS Trust —Harlow
- £39,959 - £48,117 a year
- Remote
- Management
- Mentoring
- Medical terminology
10d
Quality Manager
Communitas Clinics —Croydon
- Up to £55,000 a year
- Full-time
- Hybrid work
- Data analysis skills
- Analysis skills
- Continuous improvement
Quick apply
Diagnostics Scientist (Diagnostic Assurance and Evaluation)
UK Health Security Agency —London
- £33,422 - £45,353 a year
- Part-time
- Hybrid work
- Presentation skills
- Communication skills
10d
Laboratory Administrator (Waltham Abbey, Essex)
Health Partners —Waltham Abbey
- £24,784.50 a year
- Weekend availability
- Customer service
- Continuous improvement
- Quality control
- Annual leave
Sr Product Mgr II
RELX —London
- £100,400 - £167,300 a year
- Full-time
- Bachelor's degree
- Product management
- Business
- Employee discount
- Flexible schedule
Project Management Team Lead – Clinical Trials (f/m/d)
Clariness GmbH —London
- Full-time
- English
- Continuous improvement
- Team management
- Flexible schedule
Quick apply
Clinical Trials Manager
Neurocrine Bioscience —London
- Full-time
- Computer literacy
- Data analysis skills
- Master's degree
11d
Research Regulatory Facilitator
Imperial College London —White City
- £48,246 - £58,318 a year
- Full-time
- University
- Time management
- Annual leave
Sr Product Mgr II
Elsevier —London
- £100,400 - £167,300 a year
- Full-time
- Machine learning
- Product management
- Agile
- Employee discount
- Flexible schedule
IPS Team Lead
Get Set UK 1 —Basildon
- £35,000 - £38,500 a year
- Remote
- Team management
- Travel
- In-person
- Annual leave
Quick apply
8d
Single Sponsor Clinical Project Manager II (Virology) - 1-2 days in Uxbridge (offices moving to London in May26)
Syneos - Clinical and Corporate - Prod —London
- Full-time
- PMP
- Bachelor's degree
- Organisational skills
Medical Science Liaison, Lipids – North of England, Scotland & Northern Ireland
MSD —London
- Full-time
- Microsoft Office
- Project management
- Travel
9d

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Clinical Data Manager

Cancer Research UK -
London

Apply Now

Job details

Full-time
£39,000 - £44,000 a year
1 day ago

Qualifications

Nursing
Clinical research
Data quality analysis
Data management
Organisational skills
Good Clinical Practice (GCP)
Communication skills
Good Clinical Practice (ICH-GCP) guidelines

Full job description

Transformative methods. Inquisitive minds. Life-changing foresight.

Clinical Data Manager
£39,000 – £44,000 plus benefits

Reports to: Data Management Operations Manager
Directorate: Research & Innovation
Contract: 24-month Fixed Term Contract
Hours: Full time, 35 hours per week or a 4 day week of 28 hours.
Location: Stratford, London (high flex 1-2 days per week) or home based, UK ( at request ).
Closing date: Sunday 30th August 23:55pm
Interview date: Approximately w/c 14th September
Recruitment process: Competency based interview via Microsoft Teams + Data Management Task

Visa sponsorship: You must be eligible to work in the UK to apply for this vacancy. Cancer Research UK is not able to offer visa sponsorship.

At Cancer Research UK, we exist to beat cancer.

Cancer Research UK (CRUK) are looking for a Clinical Data Manager to join our team within our Centre for Drug Development (CDD) on a 24 month fixed term contract.

CDD is the sponsor of early phase and precision medicine clinical trials in oncology agents. Our broad portfolio rivals that of a medium-sized pharmaceutical company, spanning antibodies, cell therapies, vaccines, drug conjugates and small molecules, making this an interesting and dynamic area to work in. It is an exciting time for CDD as we’re expanding our teams to move forward with an ambitious new strategy to maximise the impact of our research to benefit patients. Several teams are hiring new roles to make this new strategy a reality, expanding the size of our project portfolio and bringing in new skills as we work more internationally.

This is a great opportunity for an experienced Clinical Data Manager, with a keen interest in the field of Oncology, to join a small team made up of 8 Data Management professionals. This will allow you to work on DETERMINE, our multi-drug, precision medicine platform trial in rare cancers, recruiting both adults and children.

What will I be doing?

Lead the data management of assigned arms of the DETERMINE trial.
Review the clinical trial data ensuring that data cleaning is managed effectively and efficiently, highlighting any issues that may affect data quality.
Manage the development or amendment of clinical trial databases, reviewing eCRFs, specifying edit checks and performing validation.
Facilitate the reporting of the data by managing the specification and validation of data listings and tables, coding adverse event terms and reconciling serious adverse events.
Monitor the status of data entry and data cleaning, locking data when appropriate to protect data integrity.
Work to achieve key performance indicators and project goals.

What are we looking for?

You will be a biomedical science graduate, hold a nursing qualification or have equivalent relevant experience.
Proven knowledge and understanding of clinical data management and drug development, working to ICH/GCP and relevant legislation.
Good knowledge and previous use of an electronic data capture (EDC) clinical trial database.
Excellent written and verbal communication skills.
Excellent attention to detail whilst retaining sight of the bigger picture.
Good planning and organisational skills, able to prioritise and manage multiple competing tasks whilst working to challenging timelines.
In addition, experience of working on oncology trials would be desirable.

Our organisation values are designed to guide all that we do.

Bold: Act with ambition, courage and determination

Credible: Act with rigour and professionalism

Human: Act to have a positive impact on people

Together: Act inclusively and collaboratively

We’re looking for people who can believe in and embody these organisation values and can use them to drive forward progress against our mission to beat cancer.

If you’re interested in applying and excited about working with us but are unsure if you have the right skills and experience, we’d still love to hear from you.

What will I gain?

We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools. Our policies and processes enable you to improve your work-life balance, take positive steps in your career and achieve your personal wellbeing goals.

You can explore our benefits by visiting our careers web page .

How do I apply?

We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won’t be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you fairly and objectively.

For more information on this career opportunity please visit our website or contact us at [email protected] .

For more updates on our work and careers, follow us on: Linked In , Facebook , Instagram , X and YouTube .

Our vision is to create a charity where everyone feels like they belong, benefits from and participates in, the work we do. We actively encourage applications from people of all backgrounds and cultures, in particular those from ethnic minority backgrounds who are currently under-represented.

We want to see every candidate performing at their best throughout the job application process, interview process and whilst at work. We therefore ask you to inform us of any concerns you have or any adjustments you might need to enable this to happen. Please contact [email protected] or 0 20 3469 8400 as soon as possible.

Unfortunately, we are unable to recruit anyone below the age of 18, so that we can protect young people from health & safety and safeguarding risks.

Apply Now

Refine Your Search

clinical data manager jobs in loughton roding, ess

Clinical Data Manager

Quality Director

Project Coordinator, Data Monitoring - Entry Level

Quality and Locations Compliance Officer

Clinical Trial Study Manager (1 Year FTC)

Head of Clinical Operations

eClinical Coordinator (London, Entry Level)

Junior Project Manager

Clinical Coding Specialist Health Group Lead (Remote/Home Working available, 20% R&R and 5% Fringe)

Quality Manager

Diagnostics Scientist (Diagnostic Assurance and Evaluation)

Laboratory Administrator (Waltham Abbey, Essex)

Sr Product Mgr II

Project Management Team Lead – Clinical Trials (f/m/d)

Clinical Trials Manager

Research Regulatory Facilitator

Sr Product Mgr II

IPS Team Lead

Single Sponsor Clinical Project Manager II (Virology) - 1-2 days in Uxbridge (offices moving to London in May26)

Medical Science Liaison, Lipids – North of England, Scotland & Northern Ireland

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