Clinical research Work, Jobs in Colwick, Ntt (with Salaries)

Clinical Research Associate
IQVIA —Nottingham
- No degree
- Travel
Clinical Research Site Lead
Civia Health —Nottingham
- Full-time
- Management
- Microsoft Office
- Supervising experience
Quick apply
Research Associate/Fellow (Fixed-Term)
University of Nottingham —Nottingham
- £32,080 - £50,253 a year
- Full-time
- Hybrid work
- Doctoral degree
- Employee discount
Research Associate/Fellow: Responsive hydrogels for targeting brain tumours (Fixed-Term)
University of Nottingham —Nottingham
- £32,080 - £35,608 a year
- Full-time
- Doctoral degree
- University
8d
Research Governance Manager
University of Nottingham —Nottingham
- £46,049 - £58,225 a year
- Full-time
1d
RTSM Solutions Architect - New Build/Amendments
4G Clinical, LLC —Nottingham
- Full-time
- Bachelor's degree
- IT
Quick apply
Software Integrations Lead
4G Clinical, LLC —Nottingham
- Full-time
- Project management
- Bachelor's degree
- IT
Quick apply

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Clinical Research Site Lead
Civia Health —Nottingham
At least 1–2 years of management or supervisory experience in a clinical or healthcare setting. Minimum of 5 years of experience in clinical research,…
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Clinical Lead/ Deputy Manager
Active Care Group —Nottingham
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11d

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clinical research jobs near colwick, ntt

Clinical Research Associate

IQVIA -
Nottingham

Apply Now

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

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clinical research jobs in colwick, ntt

Clinical Research Associate

Clinical Research Site Lead

Research Associate/Fellow (Fixed-Term)

Research Associate/Fellow: Responsive hydrogels for targeting brain tumours (Fixed-Term)

Research Governance Manager

RTSM Solutions Architect - New Build/Amendments

Software Integrations Lead

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