Clinical trials Work, Jobs in Hadfield, Dby (with Salaries)

Clinical Research Associate
IQVIA —Manchester
- Full-time
- No degree
- Travel
Anatomical Pathology Technician
The Christie NHS Foundation Trust —Manchester
- £32,073 - £39,043 a year
- Full-time
4d
Healthcare Scientist Support Worker/ Medical Laboratory Assistant
UK Health Security Agency —Manchester
- £25,651 - £27,220 a year
- Part-time
- Laboratory experience
- Presentation skills
- Data entry
6d
Clinical Research Associate II, Oncology
IQVIA —Manchester
- Full-time
- No degree
- Travel
11d
Tissue Bank Technician
The Christie NHS Foundation Trust —Manchester
- £32,073 - £39,043 a year
- Full-time
- Laboratory experience
- Travel
- IT
- Annual leave
4d
Clinical Operations Administrator
NorthWest EHealth Limited —Manchester
- £27,251 a year
- Temporary
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
- Flexible schedule
Quick apply
Field Medical Advisor / MSL - United Kingdom
Syneos Health Commercial Solutions —Manchester
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Agile Clinical Research Nurse
EMS Healthcare —Sheffield
- £42,000 - £45,000 a year
- Hybrid work
- Travel
- Organisational skills
- Agile
- Annual leave
Quick apply
10d
Theatre Practitioner
The Christie NHS Foundation Trust —Manchester
- £32,073 - £39,043 a year
- Full-time
5d
Field Medical Advisor / MSL - United Kingdom
サイネオス・ヘルス —Manchester
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Cancer Information and Support Coordinator
Weston park cancer charity —Sheffield
- £22,575.20 - £25,396.80 a year
- Part-time
- Presentation skills
- In-person
- Communication skills
- Sick pay
Quick apply
11d
Research Associate
Adelphi Group Limited —Bollington
- Hybrid work
- Microsoft Office
- Master's degree
- Bachelor's degree
- Gym membership
Quick apply
1d
Senior Research Associate
Omnicom Health —Bollington
- Hybrid work
- Microsoft Office
- Master's degree
- Bachelor's degree
- Gym membership
10d
Senior Research Associate
Adelphi Group Limited —Bollington
- Hybrid work
- Microsoft Office
- Master's degree
- Bachelor's degree
- Gym membership
Quick apply
10d
Approvals Quality Control Manager
Health Research Authority —Manchester
- £49,387 - £56,515 a year
- Full-time
- Remote
- AI
4d
Research Portfolio Manager
The Christie NHS Foundation Trust —Manchester
- £39,959 - £48,117 a year
- Full-time
- Project management
- Organisational skills
- Business
4d
Senior Clinical Research Associate, Oncology
IQVIA —Manchester
- Full-time
- No degree
11d
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
2d
Financial Management Assistant
The Christie NHS Foundation Trust —Manchester
- £28,392 - £31,157 a year
- Full-time
- IT
- Communication skills
- Flexitime
4d
Research Nurse - Cancer
East Lancashire Hospitals NHS Trust —Burnley
- £32,073 - £48,117 a year
- Part-time
- Nursing
- Communication skills
1d

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clinical trials jobs near hadfield, dby

Clinical Research Associate

IQVIA -
Manchester

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Job details

Full-time

Qualifications

Project implementation

Full job description

Manchester, 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 trials jobs in hadfield, dby

Clinical Research Associate

Anatomical Pathology Technician

Healthcare Scientist Support Worker/ Medical Laboratory Assistant

Clinical Research Associate II, Oncology

Tissue Bank Technician

Clinical Operations Administrator

Field Medical Advisor / MSL - United Kingdom

Agile Clinical Research Nurse

Theatre Practitioner

Field Medical Advisor / MSL - United Kingdom

Cancer Information and Support Coordinator

Research Associate

Senior Research Associate

Senior Research Associate

Approvals Quality Control Manager

Research Portfolio Manager

Senior Clinical Research Associate, Oncology

Booking Co-ordinator FTC

Financial Management Assistant

Research Nurse - Cancer

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