Clinical research associate Work, Jobs in Somercotes, 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
4d
Research Fellow/Associate (Fixed-Term)
University of Nottingham —Nottingham
- £32,080 - £50,253 a year
- Full-time
- Hybrid work
- Doctoral degree
- Employee discount
1d
Research Fellow (Fixed-term)
University of Nottingham —Nottingham
- £35,608 - £47,389 a year
- Full-time
- Doctoral degree
- University
- Python
- Employee discount
11d

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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
4d
Project Support Officer - Capital
Nottingham University Hospitals NHS Trust —Nottingham
Additionally, they will develop improved systems for capturing information on assets, reducing backlog, and reporting all Government-requested data—such as ERIC…
£28,392 - £31,157 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.

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