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

Clinical Research Associate
IQVIA —Nottingham
- Full-time
- No degree
- Travel
Research Assistant Custom Additive Manufacturing Hardware (Medical Applications)
Loughborough University —Loughborough
- £29,588 a year
- Full-time
- Hybrid work
- Engineering
- Master's degree
- University
7d
Clinical Trial Manager
Neupulse —Nottingham
- £45,000 - £50,000 a year
- Full-time
- Hybrid work
- Project management
- University
Quick apply
11d
Follow Up Coordinator (Fixed Term)
University of Nottingham —Nottingham
- £32,080 - £35,608 a year
- Hybrid work
- University
- Employee discount
6d
Probe Lab Engineer - Probe Repair, Testing and Innovation
Modality Group Limited —Loughborough
- Up to £35,000 a year
- Full-time
- Engineering
- Laboratory experience
- Maintenance
- Free parking
Quick apply
Children & Young People’s Independent Sexual Violence Advisor
Imara —Nottingham
- £28,119 - £28,634 a year
- Full-time
- Travel
10d
Clinical Research Site Lead
Civia Health —Nottingham
- Full-time
- Management
- Microsoft Office
- Supervising experience
Quick apply
Medicines Management Pharmacy Technician (Clinical)
Leicestershire Partnership NHS Trust —Leicester
- £29,970 - £36,483 a year
- Weekend availability
- IT
- Communication skills
5d
Solicitor or Equivalent (Clinical Negligence Grade C - Nottingham)
Fletchers Solicitors —Nottingham
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Office
- Organisational skills
- Work from home
- Sick pay
Quick apply
5d
Approvals Quality Control Manager
Health Research Authority —Nottingham
- £49,387 - £56,515 a year
- Full-time
- Remote
- AI
16h
Senior Project Manager, Immuno-Oncology and Cell and Gene Therapy
IQVIA —Nottingham
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
5d
Family Support Worker
Pasic —Leicester
- £24,800 - £26,500 a year
- Part-time
- Hybrid work
- Bilingual
- Microsoft Excel
- Microsoft Outlook
Quick apply
4d
Clinical Negligence Solicitor
Nelsons —Leicester
- Full-time
- Hybrid work
- IT
- Annual leave
- Employee discount
Production Manager
Quadralene Ltd. —Derby
- Hybrid work
- Engineering
- ERP systems
- Analysis skills
Pharmaceutical Buyer
Durbin PLC (UK) —Derby
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Spanish
Quick apply
7d
Research Governance Manager
University of Nottingham —Nottingham
- £46,049 - £58,225 a year
- Full-time
Multi-skilled engineer
Almac Group —Loughborough
- Full-time
- Engineering
- Maintenance
- English
Logistics Coordinator
Durbin PLC (UK) —Derby
- Full-time
- Microsoft Excel
- ERP systems
- Microsoft Office
Quick apply
Consultant in Ophthalmology
Contigo Healthcare —Nottingham
- £105,504 - £139,882 a year
- Full-time
- Relocation assistance
Quick apply
Software Integrations Lead
4G Clinical, LLC —Nottingham
- Full-time
- Project management
- Bachelor's degree
- IT
Quick apply

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clinical trial jobs near cotgrave, ntt

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.

Where you'll work

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

clinical trial jobs in cotgrave, ntt

Clinical Research Associate

Research Assistant Custom Additive Manufacturing Hardware (Medical Applications)

Clinical Trial Manager

Follow Up Coordinator (Fixed Term)

Probe Lab Engineer - Probe Repair, Testing and Innovation

Children & Young People’s Independent Sexual Violence Advisor

Clinical Research Site Lead

Medicines Management Pharmacy Technician (Clinical)

Solicitor or Equivalent (Clinical Negligence Grade C - Nottingham)

Approvals Quality Control Manager

Senior Project Manager, Immuno-Oncology and Cell and Gene Therapy

Family Support Worker

Clinical Negligence Solicitor

Production Manager

Pharmaceutical Buyer

Research Governance Manager

Multi-skilled engineer

Logistics Coordinator

Consultant in Ophthalmology

Software Integrations Lead

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