Clinical trial administrator Work, Jobs in Chalfont Saint Giles, Eng (with Salaries)

Clinical Registry Coordinator - UK Based
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Work from home
6d
Senior Clinical Trial Administrator
GE HEALTHCARE —Chalfont Saint Giles
- Travel
- Communication skills
Clinical Trials Administrator x2
Imperial College London —White City
- £41,005 - £45,616 a year
- Part-time
- Administrative experience
6d
Clinical Registry Coordinator
ICON Plc —Reading
- Full-time
- Remote
- Microsoft Office
- Project management
- Bachelor's degree
- Employee assistance programme
6d
Drug Safety Associate II
Corbus Pharmaceuticals Inc —London
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Nursing
Quick apply
Senior HR Administrator
Fitzrovia Hospital —London
- £30,000 - £35,000 a year
- Full-time
- Hospital
- Microsoft Office
- Human resources
- Annual leave
- Sick pay
Quick apply
Senior Principal Programmer (UK)
UCB —Slough
- Azure
- Laboratory experience
9d
Clinical Research Senior Administrator
The Royal Marsden NHS Foundation Trust —Sutton
- £36,943 - £44,900 a year
- Full-time
2d

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clinical trial administrator jobs near chalfont saint giles, eng

Clinical Registry Coordinator - UK Based

IQVIA -
Reading

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Job details

Full-time
6 days ago

Benefits

Work from home

Qualifications

Clinical research
Bachelor's degree

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.

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clinical trial administrator jobs in chalfont saint giles, eng

Clinical Registry Coordinator - UK Based

Senior Clinical Trial Administrator

Clinical Trials Administrator x2

Clinical Registry Coordinator

Drug Safety Associate II

Senior HR Administrator

Senior Principal Programmer (UK)

Clinical Research Senior Administrator

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