Clinical associate Work, Jobs in Huddersfield, Wyk (with Salaries)

CRA2 - Multi-Sponsor Department
IQVIA —Leeds
- Full-time
- Remote
- No degree
- Work from home
Clinical Research Associate
IQVIA —Manchester
- Full-time
- No degree
- Travel
Clinical Research Associate II
IQVIA —Manchester
- Full-time
- No degree
Intensive Supervision Court Key Worker
Together Women —Leeds
- £29,113 a year
- Full-time
- Microsoft Office
- Administrative experience
- Mentoring
- Employee assistance programme
- Sick pay
Quick apply
14d
Research Associate - Post stroke communication disorders
University of Sheffield —Sheffield
- £38,784 - £47,389 a year
- Part-time
- Hybrid work
- Google Suite
- Doctoral degree
- English
- Annual leave
- Employee discount
CRA 2 - Single Sponsor Dedicated
IQVIA —Manchester
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
CNN Band 4 Nurse Associate
Locala Health and Wellbeing —Liversedge
- £28,392 - £31,157 a year
- Weekend availability
- Travel
- Communication skills
- Referral programme
9d
PLOS Medicine Associate Editor- 12 Month FTC
Public Library of Science —Manchester
- £35,000 - £47,000 a year
- Remote
- Doctoral degree
- Communication skills
Clinical Territory Associate
Intuitive Surgical —Manchester
- Day shift
- Up to 50% travel
- Sales
- English
1d
Associate Case Manager
Active Care Group —Bury
- £45 an hour
- Full-time
- Microsoft Word
- Microsoft Outlook
- Travel
Quick apply
Research Associate in Causal Inference
The University of Manchester —Manchester
- £37,694 - £46,049 a year
- Hybrid work
- Doctoral degree
- Data analysis skills
- Presentation skills
- Annual leave
1d
Associate Lecturer in Food and Nutrition (permanent zero hours)
Sheffield Hallam University —Sheffield
- £39,906 - £44,746 a year
- Part-time
14d
Clinical Dietetic Manager (XR08)
Leeds Teaching Hospitals NHS Trust —Leeds
- £57,528 - £64,750 a year
- Full-time
- Management
- Leadership
- Teaching
2d
Bank Biomedical Scientist
Spire Healthcare —Manchester
- Laboratory experience
- Microsoft Office
- Business development
- Annual leave
3d
Data Systems and Information Officer
East Lancashire Hospitals NHS Trust —Accrington
- £32,073 - £39,043 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
7d
Biomedical Scientist
Spire Healthcare —Manchester
- Full-time
- Laboratory experience
- Free parking
- Annual leave
Senior Biomedical Scientist Training Lead
Spire Healthcare —Manchester
- Part-time
- Laboratory experience
- Free parking
- Annual leave
Associate SpLD Assessor
Spectrum Life —Manchester
- Communication skills
Quick apply
Service Manager - Transplant Services
Manchester University NHS Foundation Trust —Manchester
- £57,528 - £64,750 a year
- Full-time
- University
- Driving
- Organisational skills
10d
Associate Occupational Therapist
Smart Rehabilitation —Sheffield
- £40 an hour
- In-person
Quick apply

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CRA2 - Multi-Sponsor Department

IQVIA -
Leeds

Apply Now

Job details

Full-time

Benefits

Work from home

Qualifications

Clinical research
Project implementation

Full job description

Leeds, 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

clinical associate jobs in huddersfield, wyk

CRA2 - Multi-Sponsor Department

Clinical Research Associate

Clinical Research Associate II

Intensive Supervision Court Key Worker

Research Associate - Post stroke communication disorders

CRA 2 - Single Sponsor Dedicated

CNN Band 4 Nurse Associate

PLOS Medicine Associate Editor- 12 Month FTC

Clinical Territory Associate

Associate Case Manager

Research Associate in Causal Inference

Associate Lecturer in Food and Nutrition (permanent zero hours)

Clinical Dietetic Manager (XR08)

Bank Biomedical Scientist

Data Systems and Information Officer

Biomedical Scientist

Senior Biomedical Scientist Training Lead

Associate SpLD Assessor

Service Manager - Transplant Services

Associate Occupational Therapist

I want to receive the latest job alerts for clinical associate in huddersfield, wyk

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