Clinical trial Work, Jobs in Whitwell, Dby (with Salaries)

Clinical Research Associate
IQVIA —Chesterfield
- Full-time
- No degree
- Travel
Research Support Officer
Nottinghamshire Healthcare NHS Foundation Trust —Nottingham
- £32,073 - £39,043 a year
- Part-time
- University
- Driving
- Travel
9d
Approvals Quality Control Manager
Health Research Authority —Nottingham
- £49,387 - £56,515 a year
- Full-time
- Remote
- AI
20h
Research Associate/Fellow (Fixed-Term)
University of Nottingham —Nottingham
- £32,080 - £50,253 a year
- Full-time
- Hybrid work
- Doctoral degree
- Employee discount
5d
Research Assistant - Clinical Respiratory Physiologist (Part-time, Fixed term)
University of Nottingham —Nottingham
- £32,080 - £35,608 a year
- Part-time
- Hybrid work
- No degree
- Employee discount
13d
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
3h
Cancer Information and Support Coordinator
Weston park cancer charity —Sheffield
- £22,575.20 - £25,396.80 a year
- Part-time
- Presentation skills
- In-person
- Communication skills
- Sick pay
Quick apply
8d
Consultant in Ophthalmology
Contigo Healthcare —Nottingham
- £105,504 - £139,882 a year
- Full-time
- Relocation assistance
Quick apply
1d
Agile Clinical Research Nurse
EMS Healthcare —Sheffield
- £42,000 - £45,000 a year
- Hybrid work
- Travel
- Organisational skills
- Agile
- Annual leave
Quick apply
6d
Professor in Medical Statistics and Academic Lead for Clinical Trials in Oncology
University of Sheffield —Sheffield
- £71,566 - £75,915 a year
- Full-time
- Hybrid work
- Supervising experience
- Mentoring
- Leadership
- Annual leave
- Employee discount
RTSM Solutions Architect - New Build/Amendments
4G Clinical, LLC —Nottingham
- Full-time
- Bachelor's degree
- IT
Quick apply
Campaigns Manager
Weston Park Cancer Charity —Sheffield
- £32,889 - £38,978 a year
- Full-time
- Hybrid work
- CRM software
- Project management
- Marketing
- Annual leave
- Work from home
Quick apply
RTSM Study Project Lead - Level 1
4G Clinical, LLC —Nottingham
- Full-time
- Customer service
- Bachelor's degree
- IT
Quick apply
Consultant Dermatology
Contigo Healthcare —Nottingham
- Up to £20,000 a year
- Full-time
- Supervising experience
- Relocation assistance
Quick apply
1d
Software Integrations Lead
4G Clinical, LLC —Nottingham
- Full-time
- Project management
- Bachelor's degree
- IT
Quick apply

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Find similar jobs that you might be interested in.

Research Support Officer
Nottinghamshire Healthcare NHS Foundation Trust —Nottingham
The post will require travel across Trust sites within the East Midlands – the post-holder should hold a full UK driving license and have access to their own…
£32,073 - £39,043 a year
9d
Research Officer (INTERNAL ONLY) x2
University of Lincoln —Lincoln
You will work closely with colleagues to safeguard the delivery of funded research through the provision of effective and informed administrative support and…
From £28,031 a year
4h

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Clinical Research Associate

IQVIA -
Chesterfield

Apply Now

Job details

Full-time

Qualifications

Project implementation

Full job description

Chesterfield, 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 whitwell, dby

Clinical Research Associate

Research Support Officer

Approvals Quality Control Manager

Research Associate/Fellow (Fixed-Term)

Research Assistant - Clinical Respiratory Physiologist (Part-time, Fixed term)

Records Management Specialist

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

Cancer Information and Support Coordinator

Consultant in Ophthalmology

Agile Clinical Research Nurse

Professor in Medical Statistics and Academic Lead for Clinical Trials in Oncology

RTSM Solutions Architect - New Build/Amendments

Campaigns Manager

RTSM Study Project Lead - Level 1

Consultant Dermatology

Software Integrations Lead

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