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

Clinical Research Associate
IQVIA —Nottingham
- 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
Research Fellow
Sheffield Hallam University —Sheffield
- £39,906 - £44,746 a year
- Full-time
- University
7d
Researcher (0.5 FTE)
Sheffield Hallam University —Sheffield
- £32,060 - £38,784 a year
- Part-time
- Communication skills
8d
Casual Research Associate - Physical Activity Clinical Champions
Sheffield Hallam University —Sheffield
- Full-time
- No degree
2d
Research Associate/Fellow (Fixed-Term)
University of Nottingham —Nottingham
- £32,080 - £50,253 a year
- Full-time
- Hybrid work
- Doctoral degree
- Employee discount
5d
Approvals Quality Control Manager
Health Research Authority —Nottingham
- £49,387 - £56,515 a year
- Full-time
- Remote
- AI
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
Research Delivery Nurse/AHP/Officer
Nottinghamshire Healthcare NHS Foundation Trust —Nottingham
- £32,073 - £39,043 a year
- Full-time
- Driving
- Communication skills
8d
Lead Technical Expert: Clinical Radiation
Health Research Authority —Nottingham
- £113,565 - £150,569 a year
- Part-time
- Hybrid work
- AI
- Leadership
6d
Research Fellow (Fixed-term)
University of Nottingham —Nottingham
- £35,608 - £47,389 a year
- Full-time
- Doctoral degree
- University
- Python
- Employee discount
Research Technician
University of Sheffield —Sheffield
- £27,319 a year
- Full-time
- Hybrid work
- Data analysis skills
- Laboratory experience
- Master's degree
- Annual leave
- Employee discount
1d
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
Consultant Clinical Psychologist
MEDI SPEC LTD —Sheffield
- £100 an hour
- Part-time
- Hybrid work
- Bachelor's degree
- Patient care
- Communication skills
Quick apply
9d
RTSM Solutions Architect - New Build/Amendments
4G Clinical, LLC —Nottingham
- Full-time
- Bachelor's degree
- IT
Quick apply
Restaurant Staff Member
chesters Ltd —Chesterfield
- £12.44 - £14.00 an hour
- Part-time
- Data analysis skills
- SQL
- Analysis skills
Quick apply
13d
Software Integrations Lead
4G Clinical, LLC —Nottingham
- Full-time
- Project management
- Bachelor's degree
- IT
Quick apply

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Clinical Research Associate
IQVIA —Nottingham
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)…
Clinical Trials Co-ordinator
Manchester University NHS Foundation Trust —Manchester
Your role will be to co-ordinate studies within Research & Innovation (R&I) and t o ensure that comprehensive, high quality and efficient administrative…
£32,073 - £39,043 a year
2d

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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 research jobs in heage, dby

Clinical Research Associate

Research Support Officer

Research Fellow

Researcher (0.5 FTE)

Casual Research Associate - Physical Activity Clinical Champions

Research Associate/Fellow (Fixed-Term)

Approvals Quality Control Manager

Agile Clinical Research Nurse

Research Delivery Nurse/AHP/Officer

Lead Technical Expert: Clinical Radiation

Research Fellow (Fixed-term)

Research Technician

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

Consultant Clinical Psychologist

RTSM Solutions Architect - New Build/Amendments

Restaurant Staff Member

Software Integrations Lead

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