Clinical trial Work, Jobs in Chesterfield, Eng (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
8d
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
7d
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
12d
Research Fellow/Associate (Fixed-Term)
University of Nottingham —Nottingham
- £32,080 - £50,253 a year
- Full-time
- Hybrid work
- Doctoral degree
- Employee discount
4d
Consultant in Ophthalmology
Contigo Healthcare —Nottingham
- £105,504 - £139,882 a year
- Full-time
- Relocation assistance
Quick apply
21h
Records Management Specialist
Perceptive —Nottingham
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
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
Director, Scientific Product Development
Catalent —Nottingham
- Full-time
Agile Clinical Research Nurse
EMS Healthcare —Sheffield
- £42,000 - £45,000 a year
- Hybrid work
- Travel
- Organisational skills
- Agile
- Annual leave
Quick apply
5d
Clinical Account Manager
Getinge Ltd. —Derby
- Weekend availability
- English
- Microsoft Office
- Presentation skills
- Employee assistance programme
- Employee discount
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
Facilities Engineer
Catalent —Nottingham
- Full-time
- Maintenance
- English
- Microsoft Office
- Free parking
- Employee assistance programme
Cleaning Technician
Catalent —Nottingham
- Full-time
- Organisational skills
- Communication skills
- Free parking
- Employee assistance programme
Software Integrations Lead
4G Clinical, LLC —Nottingham
- Full-time
- Project management
- 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
21h
RTSM Solutions Architect - New Build/Amendments
4G Clinical, LLC —Nottingham
- Full-time
- Bachelor's degree
- IT
Quick apply
RTSM Study Project Lead - Level 1
4G Clinical, LLC —Nottingham
- Full-time
- Customer service
- Bachelor's degree
- IT
Quick apply

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Clinical Research Associate
IQVIA —Chesterfield
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)…
Research Assistant (Wellcome)
University of Sheffield —Sheffield
We offer a fantastic range of benefits including a highly competitive annual leave entitlement (with the ability to purchase more), a generous pensions scheme,…
£32,080 - £33,951 a year
8d

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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 chesterfield, eng

Clinical Research Associate

Research Support Officer

Cancer Information and Support Coordinator

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

Research Fellow/Associate (Fixed-Term)

Consultant in Ophthalmology

Records Management Specialist

Campaigns Manager

Director, Scientific Product Development

Agile Clinical Research Nurse

Clinical Account Manager

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

Facilities Engineer

Cleaning Technician

Software Integrations Lead

Consultant Dermatology

RTSM Solutions Architect - New Build/Amendments

RTSM Study Project Lead - Level 1

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