Clinical research Work, Jobs in Tideswell, Dby (with Salaries)

Clinical Research Associate
IQVIA —Chesterfield
- No degree
- Travel
Lead Clinical Research Practitioner & Portfolio Co-ordinator
Manchester University NHS Foundation Trust —Manchester
- £39,959 - £48,117 a year
- Full-time
- Hybrid work
- Patient monitoring
- University
- Organisational skills
5d
Research Associate
University of Sheffield —Sheffield
- £38,784 - £41,064 a year
- Full-time
- Hybrid work
- Doctoral degree
- University
- IT
- Annual leave
- Employee discount
Research Associate - Post stroke communication disorders
University of Sheffield —Sheffield
- £38,784 - £47,389 a year
- Part-time
- Hybrid work
- Google Suite
- Doctoral degree
- English
- Annual leave
- Employee discount
10d
Clinical Research Associate II
IQVIA —Manchester
- No degree
12d
Research Support Officer
Manchester University NHS Foundation Trust —Manchester
- £28,392 - £31,157 a year
- Full-time
- Microsoft Excel
- University
- AI
5d
Biobank Technician
The University of Manchester —Manchester
- £33,002 - £33,951 a year
- Hybrid work
- Laboratory experience
- IT
- Communication skills
- Annual leave
- Employee discount
4d
Senior Paediatric Clinical Research Nurse CRF RMCH
Manchester University NHS Foundation Trust —Manchester
- £39,959 - £48,117 a year
- Full-time
- University
- AI
- Communication skills
5d
Clinical Research Matron
The Christie NHS Foundation Trust —Manchester
- £57,528 - £64,750 a year
- Weekend availability
Research Technician - Grade 4
The University of Manchester —Manchester
- £29,588 - £32,080 a year
- Full-time
- Hybrid work
- University
- Annual leave
- Employee assistance programme
2d
Senior Scientist I
Charles River Laboratories —High Peak
- Full-time
- Doctoral degree
- Sales
- Laboratory experience
Clinical Research Nurse
The Christie NHS Foundation Trust —Manchester
- £39,959 - £48,117 a year
- Part-time
- Maintenance
- Organisational skills
- IT
4d
Senior Trial Manager Research Fellow or Senior Research Fellow
University of Sheffield —Sheffield
- £48,822 - £80,254 a year
- Full-time
- Hybrid work
- Supervising experience
- Mentoring
- Leadership
- Annual leave
- Employee discount
12d
Transition Fellow
The University of Manchester —Manchester
- £47,389 - £58,225 a year
- Call to connect
- Hybrid work
- Doctoral degree
- University
- Annual leave
- Employee assistance programme
Director, Patient Centered Outcomes Assessment
RTI International —Manchester
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Presentation skills
4d
Research Project Manager
The Christie NHS Foundation Trust —Manchester
- £39,959 - £48,117 a year
- Full-time
- Project management
- Organisational skills
- Leadership
2d
Sr. CRA 1 - Site Management
IQVIA —Manchester
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Research Associate in Nanomedicine
The University of Manchester —Manchester
- £37,694 - £46,049 a year
- Hybrid work
- Doctoral degree
- Annual leave
11d
Research Project Manager
The University of Manchester —Manchester
- £37,694 - £41,064 a year
- Hybrid work
- Project management
- No degree
- Organisational skills
- Annual leave
6d
CRA 2 - Single Sponsor Dedicated
IQVIA —Manchester
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel

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clinical research jobs near tideswell, dby

Clinical Research Associate

IQVIA -
Chesterfield

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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 research jobs in tideswell, dby

Clinical Research Associate

Lead Clinical Research Practitioner & Portfolio Co-ordinator

Research Associate

Research Associate - Post stroke communication disorders

Clinical Research Associate II

Research Support Officer

Biobank Technician

Senior Paediatric Clinical Research Nurse CRF RMCH

Clinical Research Matron

Research Technician - Grade 4

Senior Scientist I

Clinical Research Nurse

Senior Trial Manager Research Fellow or Senior Research Fellow

Transition Fellow

Director, Patient Centered Outcomes Assessment

Research Project Manager

Sr. CRA 1 - Site Management

Research Associate in Nanomedicine

Research Project Manager

CRA 2 - Single Sponsor Dedicated

I want to receive the latest job alerts for clinical research in tideswell, dby

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