Clinical research associates & coordinators Work, Jobs in Parbold, Lan (with Salaries)

Clinical Research Associate
IQVIA —Manchester
- Full-time
- No degree
- Travel
Senior Clinical Research Associate
IQVIA —Manchester
- Full-time
- No degree
Clinical Trials Co-ordinator
Manchester University NHS Foundation Trust —Manchester
- £32,073 - £39,043 a year
- Part-time
- Driving
- IT
12h
Clinical Research Associate II, Oncology
IQVIA —Manchester
- Full-time
- No degree
- Travel
5d
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
Senior Clinical Trial Coordinator
The Christie NHS Foundation Trust —Manchester
- £32,073 - £39,043 a year
- Full-time
- Team management
- Business
- Leadership
11d
Agile Clinical Research Nurse
EMS Healthcare —Manchester
- £42,000 - £45,000 a year
- Hybrid work
- Travel
- Organisational skills
- Agile
- Annual leave
Quick apply
Senior Clinical Research Nurse-(OC)
Manchester University NHS Foundation Trust —Manchester
- £39,959 - £48,117 a year
- Full-time
- University
- AI
- Teaching
11d
Personal Care Clinical Hot Room Assessment Leader
Unilever —Bebington
- Full-time
- Hybrid work
- Bachelor's degree
- Communication skills
12d
Bank Clinical Research Nurse
EMS Healthcare —Preston
- Temporary
- Travel
- Organisational skills
- Communication skills
Quick apply
Senior Clinical Research Associate, Oncology
IQVIA —Manchester
- Full-time
- No degree
5d
Senior Research Project Manager (translational research)
The Christie NHS Foundation Trust —Manchester
- £49,387 - £56,515 a year
- Full-time
- Project management
4d

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clinical research associates & coordinators jobs near parbold, lan

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 research associates & coordinators jobs in parbold, lan

Clinical Research Associate

Senior Clinical Research Associate

Clinical Trials Co-ordinator

Clinical Research Associate II, Oncology

Clinical Operations Administrator

Senior Clinical Trial Coordinator

Agile Clinical Research Nurse

Senior Clinical Research Nurse-(OC)

Personal Care Clinical Hot Room Assessment Leader

Bank Clinical Research Nurse

Senior Clinical Research Associate, Oncology

Senior Research Project Manager (translational research)

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