Clinical trial Work, Jobs in Shepshed, Lec (with Salaries)

Clinical Research Associate
IQVIA —Nottingham
- Full-time
- No degree
- Travel
Project Associate, CTRx Solutions
Myonex —Leicester
- £30,000 - £36,000 a year
- Full-time
- Customer service
12d
Records Management Specialist
Perceptive —Nottingham
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Warehouse Associate
Myonex —Leicester
- £19,066.67 - £20,533.33 a year
- Part-time
- Microsoft Word
- Microsoft Outlook
- Microsoft Office
6d
Research Associate/Fellow (Fixed-Term)
University of Nottingham —Nottingham
- £32,080 - £50,253 a year
- Full-time
- Hybrid work
- Doctoral degree
- Employee discount
9d
Approvals Quality Control Manager
Health Research Authority —Nottingham
- £49,387 - £56,515 a year
- Full-time
- Remote
- AI
4d
Clinical Research Site Lead
Civia Health —Nottingham
- Full-time
- Management
- Microsoft Office
- Supervising experience
Quick apply
2d
Project Manager, CTRx Solutions
Myonex —Leicester
- £52,000 - £55,000 a year
- Full-time
- Management
- Customer service
Clinical Negligence Solicitor
Nelsons —Leicester
- Full-time
- Hybrid work
- IT
- Annual leave
- Employee discount
Specialist Pharmacist Clinical Trials
University Hospitals Coventry and Warwickshire NHS Trust —Coventry
- £49,387 - £56,515 a year
- Full-time
- Project management
13d
Parkinsons and Movement Disorder Fellowship
University Hospitals Coventry and Warwickshire NHS Trust —Coventry
- £67,325 a year
- Full-time
3d
Warehouse Operative - Nights
LF&E Refrigerated Transport —Ashby-De-La-Zouch
- £14,476.80 a year
- Part-time
- Employee assistance programme
3d
Specialist Pharmacist Clinical Trials (Experienced)
University Hospitals Coventry and Warwickshire NHS Trust —Coventry
- £49,387 - £56,515 a year
- Full-time
- Project management
RTSM Study Project Lead - Level 1
4G Clinical, LLC —Nottingham
- Full-time
- Customer service
- Bachelor's degree
- IT
Quick apply
Logistics Coordinator
Durbin PLC (UK) —Derby
- Full-time
- Microsoft Excel
- ERP systems
- Microsoft Office
Quick apply
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
4d
Locum Consultant Nuclear Medicine Radiologist- Radionuclide Imaging
University Hospitals Coventry and Warwickshire NHS Trust —Coventry
- £113,565 - £150,569 a year
- Full-time
3d
Software Integrations Lead
4G Clinical, LLC —Nottingham
- Full-time
- Project management
- Bachelor's degree
- IT
Quick apply
Multi Skilled Maintenance Engineer
Pharmaron —Castle Donington
- Maintenance
- Mechanical knowledge
Quick apply
Facilities Engineer
Catalent —Nottingham
- Full-time
- Maintenance
- English
- Microsoft Office
- Free parking
- Employee assistance programme

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Clinical Research Associate

IQVIA -
Nottingham

Apply Now

Job details

Full-time

Qualifications

Project implementation

Full job description

Nottingham, United Kingdom | Full time | Field-based | R1514135

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 shepshed, lec

Clinical Research Associate

Project Associate, CTRx Solutions

Records Management Specialist

Warehouse Associate

Research Associate/Fellow (Fixed-Term)

Approvals Quality Control Manager

Clinical Research Site Lead

Project Manager, CTRx Solutions

Clinical Negligence Solicitor

Specialist Pharmacist Clinical Trials

Parkinsons and Movement Disorder Fellowship

Warehouse Operative - Nights

Specialist Pharmacist Clinical Trials (Experienced)

RTSM Study Project Lead - Level 1

Logistics Coordinator

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

Locum Consultant Nuclear Medicine Radiologist- Radionuclide Imaging

Software Integrations Lead

Multi Skilled Maintenance Engineer

Facilities Engineer

I want to receive the latest job alerts for clinical trial in shepshed, lec

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