Research operations occupations Work, Jobs in Halton, Chs (with Salaries)

Clinical Research Associate
IQVIA —Manchester
- No degree
- Travel
UX Research Operations (ResOps) Specialist
interactive investor —Manchester
- £42,230 - £63,350 a year
- Full-time
- Hybrid work
- Project management
- SharePoint
- AI
- Annual leave
- Employee discount
Quick apply
10d
Technical Assurance Officer
Health Research Authority —Manchester
- £39,959 - £48,117 a year
- Full-time
- Remote
- Administrative experience
- Organisational skills
- AI
10d
Project Manager
University of Liverpool —Liverpool
- £39,906 - £46,049 a year
- Full-time
- University
4d
Research Development Officer
Manchester Metropolitan University —Manchester
- £31,236 - £34,610 a year
- Full-time
- Hybrid work
- Analysis skills
- University
- Annual leave
- Life insurance
Clinical Trials Administration Assistant
The Clatterbridge Cancer Centre NHS Foundation Trust —Liverpool
- £25,760 - £27,476 a year
- Full-time
- IT
- Communication skills
- Time management
2d
Research Midwife
Wirral University Teaching Hospital NHS Foundation Trust —Wirral
- £39,959 - £48,117 a year
- Part-time
- Computer skills
2d
CRADLE Project Manager
The University of Manchester —Manchester
- £37,694 - £46,049 a year
- Full-time
- Hybrid work
- University
- Annual leave
- Employee assistance programme
4d
Research Associate II
Thermo Fisher Scientific —Manchester
- 8 hour shift
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
3d
Market Access & Commercialisation Manager
Liverpool School of Tropical Medicine —Liverpool
- £39,906 - £43,482 a year
- Hybrid work
- Management
- Annual leave
9d
Clinical Research Fellow - Clinical Uro-Oncology
The Christie NHS Foundation Trust —Manchester
- £54,499 - £76,582 a year
- Weekend availability
Senior Enterprise Manager (Biosciences)
University of Liverpool —Liverpool
- £47,389 - £59,966 a year
- Full-time
- Hybrid work
- University
- No degree
- Communication skills
10d
R&D Group Leader
Sherwin-Williams —Bolton
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Projects & Events Administrator, African Cities Research Consortium
The University of Manchester —Manchester
- £28,031 - £31,326 a year
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
- Employee discount
Category Head R&D (OND)
Imperial Brands —Liverpool
- Engineering
3d
Senior Research Nurse
Liverpool University Hospitals NHS Foundation Trust —Liverpool
- £49,387 - £56,515 a year
- Full-time
- Project management
- Rehabilitation centre
- Leadership
5d
Booking Co-ordinator FTC
NorthWest EHealth Limited —Manchester
- Up to £27,251 a year
- Full-time
- Hybrid work
- Microsoft Outlook
- Data entry
- Organisational skills
- Annual leave
- Flexible schedule
Quick apply
Agile Trial Coordinator
EMS Healthcare —West Kirby
- Weekend availability
- Travel
- Organisational skills
- Communication skills
Quick apply
5d
Advanced Clinical Practitioner Research - Non-Malignant Haematology
Liverpool University Hospitals NHS Foundation Trust —Liverpool
- £57,528 - £64,750 a year
- Full-time
- Rehabilitation centre
- Teaching
10d
Lead Technical Expert: Clinical Radiation
Health Research Authority —Manchester
- £113,565 - £150,569 a year
- Part-time
- Hybrid work
- AI
- Leadership

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research operations occupations jobs near halton, chs

Clinical Research Associate

IQVIA -
Manchester

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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

research operations occupations jobs in halton, chs

Clinical Research Associate

UX Research Operations (ResOps) Specialist

Technical Assurance Officer

Project Manager

Research Development Officer

Clinical Trials Administration Assistant

Research Midwife

CRADLE Project Manager

Research Associate II

Market Access & Commercialisation Manager

Clinical Research Fellow - Clinical Uro-Oncology

Senior Enterprise Manager (Biosciences)

R&D Group Leader

Projects & Events Administrator, African Cities Research Consortium

Category Head R&D (OND)

Senior Research Nurse

Booking Co-ordinator FTC

Agile Trial Coordinator

Advanced Clinical Practitioner Research - Non-Malignant Haematology

Lead Technical Expert: Clinical Radiation

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