Clinical trial Work, Jobs in Arnold, Ntt (with Salaries)

Clinical Research Associate
IQVIA —Nottingham
- No degree
- Travel
Research Associate/Fellow (Fixed-Term)
University of Nottingham —Nottingham
- £32,080 - £50,253 a year
- Full-time
- Hybrid work
- Doctoral degree
- Employee discount
Clinical Research Site Lead
Civia Health —Nottingham
- Full-time
- Management
- Microsoft Office
- Supervising experience
Quick apply
Records Management Specialist
Perceptive —Nottingham
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Salaried GP in Friendly, Semi-Rural Practice - 6 sessions - 9 months fixed term Maternity Cover
Arthur Medical Centre —Ilkeston
- From £11,000 a year
- Part-time
- Anatomy knowledge
- Medication administration
- Bachelor's degree
- Annual leave
Quick apply
Production Manager
Quadralene Ltd. —Derby
- Hybrid work
- Engineering
- ERP systems
- Analysis skills
2h
Consultant in Ophthalmology
Contigo Healthcare —Nottingham
- £105,504 - £139,882 a year
- Full-time
- Relocation assistance
Quick apply
Consultant Dermatology
Contigo Healthcare —Nottingham
- Up to £20,000 a year
- Full-time
- Supervising experience
- Relocation assistance
Quick apply
Senior Pharmacy Technician
Chesterfield Royal Hospital NHS Foundation Trust —Chesterfield
- £32,073 - £39,043 a year
- Full-time
- Hospice
- Hospital experience
2d
Human Resources Business Partner
4G Clinical, LLC —Nottingham
- Full-time
- Bachelor's degree
- No degree
- Human resources
Quick apply
4d
Logistics Coordinator
Durbin PLC (UK) —Derby
- Full-time
- Microsoft Excel
- ERP systems
- Microsoft Office
Quick apply
RTSM Study Project Lead - Level 1
4G Clinical, LLC —Nottingham
- Full-time
- Customer service
- Bachelor's degree
- IT
Quick apply
RTSM Solutions Architect - New Build/Amendments
4G Clinical, LLC —Nottingham
- Full-time
- Bachelor's degree
- IT
Quick apply
Multi Skilled Maintenance Engineer
Pharmaron —Castle Donington
- Maintenance
- Mechanical knowledge
Quick apply
Multi-skilled engineer
Almac Group —Loughborough
- Full-time
- Engineering
- Maintenance
- English
3d
Software Integrations Lead
4G Clinical, LLC —Nottingham
- Full-time
- Project management
- Bachelor's degree
- IT
Quick apply
Class 2 Relief Trunk Driver and Sortation Support
LF&E Refrigerated Transport —Swadlincote
- £39,288.60 a year
- Full-time
- Warehouse experience

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Clinical Research Associate
IQVIA —Nottingham
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF)…
Clinical Trials Assistant
Sheffield Teaching Hospitals NHS Foundation Trust —Sheffield
The role will involve completing and submitting documents to the Clinical Research and Innovation Office (CRIO) obtain approvals; collecting, recording and…
£28,392 - £31,157 a year
2d

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Clinical Research Associate

IQVIA -
Nottingham

Apply Now

Job details

Qualifications

Project implementation

Full job description

IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world.

The Clinical Research Associate will support Oncology studies and cover sites across the UK

Apply today and forge a career with greater purpose, make an impact and never stop learning!

Responsibilities

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.

Requirements

Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Life science degree educated or equivalent industry experience
Flexibility to travel to sites as required

*Please note - this role is not eligible for visa sponsorship*

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Apply Now

Refine Your Search

clinical trial jobs in arnold, ntt

Clinical Research Associate

Research Associate/Fellow (Fixed-Term)

Clinical Research Site Lead

Records Management Specialist

Salaried GP in Friendly, Semi-Rural Practice - 6 sessions - 9 months fixed term Maternity Cover

Production Manager

Consultant in Ophthalmology

Consultant Dermatology

Senior Pharmacy Technician

Human Resources Business Partner

Logistics Coordinator

RTSM Study Project Lead - Level 1

RTSM Solutions Architect - New Build/Amendments

Multi Skilled Maintenance Engineer

Multi-skilled engineer

Software Integrations Lead

Class 2 Relief Trunk Driver and Sortation Support

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