Clinical research coordinator Work, Jobs in Sipson, Gtl (with Salaries)

Project Specialist - Clinical Registry Coordinator - UK Based
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Work from home
13d
Clinical Research Coordinator/Cognitive Rater
Imperial College Healthcare NHS Trust —London
- £47,951 - £56,863 a year
- Full-time
7h
eClinical Coordinator (London)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Microsoft Excel
- English
- Annual leave
Clinical Service Manager
Acacium Group —London
- £42,000 - £45,000 a year
- Full-time
- Hybrid work
- Leadership
- Employee assistance programme
Quick apply
eClinical Coordinator (London, Entry Level)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Microsoft Excel
- English
- Annual leave
Clinical Safety Coordinator
Medpace, Inc. —London
- Full-time
- Microsoft Office
- Bachelor's degree
- Medical terminology
- Annual leave
Project Coordinator - UK
Fortrea —Maidenhead
- Full-time
- English
- Communication skills
2d
Data Coordinator (London, Entry-Level)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Microsoft Excel
- English
- Annual leave
Project Coordinator, Data Monitoring - Entry Level
Medpace, Inc. —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Bachelor's degree
- Annual leave
14h
Clinical Monitoring Lead
Biogen —Maidenhead
- Full-time
- Hybrid work
- Nursing
- Bachelor's degree
- Team management
14h
Senior RA Coordinator
Novartis —London
- £32,690 - £60,710 a year
- Full-time
- Hybrid work
- Communication skills
Project Management Team Lead – Clinical Trials (f/m/d)
Clariness GmbH —London
- Full-time
- English
- Project management
- Mentoring
- Flexible schedule
Quick apply
Medical Education Administrator
Kingston and Richmond NHS Foundation Trust —London
- £33,262 - £36,027 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Outlook
- Writing skills
- Employee assistance programme
8h
Senior Coordinator
IQVIA —Reading
- Full-time
- Hybrid work
Global Medical Affairs Research Grant & Study Manager
Santen —St Albans
- £78,863 - £108,436 a year
- Full-time
- Remote
- Nursing
- Analysis skills
- Bachelor's degree
Quick apply
6d
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Team Coordinator, R&D
Compass Pathways —London
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
- Annual leave
Quick apply
Clinical Research Nurse - 12 month FTC
hVIVO Services Limited —London
- Night shift
- Nursing
- Organisational skills
- IT
Clinical Research Nurse - Bank, Full-Time
hVIVO Services Limited —London
- Night shift
- Nursing
- Organisational skills
- IT
Band 5 GCLP- Biobank Laboratory Coordinator
Royal Free London NHS Foundation Trust —London
- £38,488 - £46,852 a year
- Full-time
- Flexible schedule
7h

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Project Specialist - Clinical Registry Coordinator - UK Based

IQVIA -
Reading

Apply Now

Job details

Full-time
13 days ago

Benefits

Work from home

Qualifications

Clinical research
Stakeholder collaboration
Bachelor's degree
Data management
Pharmaceutical industry setting experience

Full job description

Reading, United Kingdom | Full time | Home-based | R1558206

Essential Functions

Provides clinical registry support, oversight, and/or accountability for one or more development programs for clinical trials.
Takes a leadership role with the clinical development team and other internal and external partners to establish, align, and confirm clinical registry expectations for assigned trial(s).
Responsible for submission of approved documents and content to registries worldwide. Submissions are made by the Clinical Registry Administrators.
Responsible for tracking, reporting, and documentation of disclosure records and associated documents in tools and systems used by the clinical registry group.
Assists business partners, external partners, and local operating companies in maintaining accurate and correct (source) data relevant to the disclosure process.
Ensures timely resolution of planning issues to ensure compliant delivery of the disclosure planning.
Ensures deliverables are on time.

Qualifications

A minimum of 4 years of relevant pharmaceutical/scientific experience in a clinical development environment (pharmaceutical, medical device, CRO, or other clinical development service organization) is required.
Bachelor’s degree in Health or Science discipline is required with experience in clinical research
Clinical Registry experience preferred.
Experience working on a clinical trial or regulatory document management preferred.

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 research coordinator jobs in sipson, gtl

Project Specialist - Clinical Registry Coordinator - UK Based

Clinical Research Coordinator/Cognitive Rater

eClinical Coordinator (London)

Clinical Service Manager

eClinical Coordinator (London, Entry Level)

Clinical Safety Coordinator

Project Coordinator - UK

Data Coordinator (London, Entry-Level)

Project Coordinator, Data Monitoring - Entry Level

Clinical Monitoring Lead

Senior RA Coordinator

Project Management Team Lead – Clinical Trials (f/m/d)

Medical Education Administrator

Senior Coordinator

Global Medical Affairs Research Grant & Study Manager

Clinical Trials Manager

Team Coordinator, R&D

Clinical Research Nurse - 12 month FTC

Clinical Research Nurse - Bank, Full-Time

Band 5 GCLP- Biobank Laboratory Coordinator

I want to receive the latest job alerts for clinical research coordinator in sipson, gtl

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