Master data Work, Jobs in Frodsham, Chs (with Salaries)

CRA2 - Multi-Sponsor Department
IQVIA —Manchester
- Full-time
- Remote
- No degree
- Work from home
Master Data Associate
Nichols PLC —Newton-le-Willows
- Hybrid work
- Microsoft Excel
- Organisational skills
- Communication skills
- Free parking
- Employee discount
5d
Master Technician / Senior Diagnostic Technician
Johnny's Garage LTD —Wrexham
- £41,000 - £43,000 a year
- Full-time
- Mentoring
- Power tools
- In-person
Quick apply
8d
Lead Automation & Integration Engineer
Power Resources International Ltd —Manchester
- £32,120.33 - £65,906.19 a year
- Full-time
- Master's degree
- JavaScript
- Mentoring
Quick apply
Global Supply Planner (Fixed-Term)
Convatec —Deeside
- Weekend availability
- Microsoft Excel
- Customer service
- Analysis skills
Assistant Editor (PhD/Master's) - Mathematics, Statistics, and Computer Science
MDPI UK —Manchester
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
- Employee discount
Planner - Supply Chain - UK & IRE
Azelis —Runcorn
- Full-time
- Organisational skills
- IT
- Communication skills
Lead Data Engineer
Northrop Grumman —Manchester
- £60,000 - £86,000 a year
- Hybrid work
- SQL
- AWS
- Travel
- Relocation assistance
Senior Advisor - Engineering Manufacturing Network Powder/Solids
Elanco —Speke
- Full-time
- Doctoral degree
- Engineering
- English
IT Business Applications (ERP) Manager
INEOS Group —Runcorn
- Full-time
- Management
- Project management
- IT
Sr. CRA 1 - Site Management
IQVIA —Manchester
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Work from home
Art Therapist
Stepping Stones North Wales —Stansty ED
- £40 an hour
- Part-time
- Hybrid work
- English
- Master's degree
- Organisational skills
Quick apply
10d
AP Freshdesk Support Analyst
Travel Counsellors —Manchester
- Hybrid work
- Microsoft Excel
- Microsoft Office
- IT
Quick apply
Operational Procurement Manager
M Group —Warrington
- Oracle
- ERP systems
- Analysis skills
- Annual leave
- Employee assistance programme
AI Engineer (KTP Associate)
Manchester Metropolitan University —Manchester
- Up to £40,740 a year
- Full-time
- Computer Science
- Master's degree
- Project management
10d
Senior Associate Global Lab Informatics
Elanco —Speke
- Full-time
- Engineering
- Laboratory experience
- Analysis skills
Director, Supply Chain
Elanco —Speke
- Full-time
- Sales
- Engineering
- Bachelor's degree
11d
Customer Supply Chain Specialist
Cereal Partners Worldwide —Wirral
- £35,000 a year
- Full-time
- Customer service
- Analysis skills
1d
Sr. Product Manager
Omnicell —Warrington
- £90,000 - £105,000 a year
- Master's degree
- Analysis skills
- Bachelor's degree
People Operations Advisor
Together Trust —Cheadle
- £36,040 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Office
- Presentation skills
- Annual leave
- Employee assistance programme
Quick apply
4d

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CRA2 - Multi-Sponsor Department

IQVIA -
Manchester

Apply Now

Job details

Full-time

Benefits

Work from home

Qualifications

Clinical research
Project implementation

Full job description

Manchester, United Kingdom | Full time | Home-based | R1530767

IQVIA UK’s Site Management (multi-sponsor) team is growing and seeking junior and experienced Clinical Research Associates.

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 regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
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
You have successfully managed multiple clinical trial protocols across diverse investigative sites.
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

Please note - this role is not eligible for UK 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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

master data jobs in frodsham, chs

CRA2 - Multi-Sponsor Department

Master Data Associate

Master Technician / Senior Diagnostic Technician

Lead Automation & Integration Engineer

Global Supply Planner (Fixed-Term)

Assistant Editor (PhD/Master's) - Mathematics, Statistics, and Computer Science

Planner - Supply Chain - UK & IRE

Lead Data Engineer

Senior Advisor - Engineering Manufacturing Network Powder/Solids

IT Business Applications (ERP) Manager

Sr. CRA 1 - Site Management

Art Therapist

AP Freshdesk Support Analyst

Operational Procurement Manager

AI Engineer (KTP Associate)

Senior Associate Global Lab Informatics

Director, Supply Chain

Customer Supply Chain Specialist

Sr. Product Manager

People Operations Advisor

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