Clinical research specialist Work, Jobs in West Byfleet, Sry (with Salaries)

Project Specialist - Clinical Registry Coordinator - UK Based
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Work from home
8d
Mindworks Hub Clinical Practitioner
Surrey and Borders Partnership NHS Foundation Trust —Chertsey
- £41,957 - £50,387 a year
- Full-time
- Care plans
- Leadership
- School
- Free parking
7d
Specialist Pharmacy Technician – Clinical Trials
Surrey and Borders Partnership NHS Foundation Trust —Chertsey
- £41,957 - £50,387 a year
- Part-time
- Travel
- Free parking
1d
Clinical Trials Assistant
University College London Hospitals NHS Foundation Trust —London
- £34,186 - £37,389 a year
- Full-time
- Microsoft Excel
- Communication skills
1d
Senior Clinical Scientist (Magnetic Resonance Physics)
University College London Hospitals NHS Foundation Trust —London
- £66,274 - £73,496 a year
- Full-time
- University
- Leadership
- Communication skills
Research Assistant
University College London Hospitals NHS Foundation Trust —London
- £38,488 - £46,852 a year
- Full-time
- Organisational skills
- Communication skills
7d
Psychological Therapist - Cognitive Behavioural Therapy (CBT)
Berkshire Healthcare NHS Foundation Trust —Bracknell
- £51,657 - £58,785 a year
- Full-time
- School
- Free parking
- Annual leave
6d
Clinical Trials Coordinator
University College London —London
- £43,981 a year
- Full-time
- Hybrid work
1d
Clinical Trials Coordinator part time 0.5 FTE
University College London —London
- £21,990.50 a year
- Part-time
- Hybrid work
1d
Medical Information Specialist - US Hours
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- English
Quick apply
Analyst - Health Technology Assessment and Outcomes Research (Fixed Term for 1 year)
MSD —London
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Project management
2d
Research Regulatory Facilitator
Imperial College London —White City
- £48,246 - £58,318 a year
- Full-time
- Administrative experience
- University
- Time management
- Annual leave
5h
Specialist Clinical Coder
Guy's and St Thomas' NHS Foundation Trust —London
- £47,951 - £56,863 a year
- Full-time
- Hybrid work
10d
Information, Knowledge, and Support Adviser (Rare Dementia Support)
University College London —London
- £43,981 - £52,586 a year
- Full-time
- Bachelor's degree
- Organisational skills
- Communication skills
- Annual leave
- Employee assistance programme
9d
Behaviour Support Practitioner
South London and Maudsley NHS Foundation Trust —London
- £47,951 - £56,863 a year
- Full-time
- Management
- Care plans
- School
9d
Clinical Scientist/Clinical Scientist - Graduate Trainee
NHS Blood and Transplant —Tooting
- £39,959 - £56,515 a year
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
- Employee assistance programme
11d
Mental Health Therapeutic Practitioner
Central and North West London NHS Foundation Trust —London
- £55,524 - £62,652 a year
- Full-time
- Communication skills
- Relocation assistance
- Employee discount
18h
Clinical Physiologist (Neurophysiology)
University College London Hospitals NHS Foundation Trust —London
- £58,133 - £65,261 a year
- Full-time
- Organisational skills
- Communication skills
9d
Clinical Research Fellow
King's College Hospital NHS Foundation Trust —London
- £67,325 a year
- Full-time
10d
Medical Doctor (UK) - Freelance AI Trainer Project
Meridial —London
- £40 - £120 an hour
- Remote
- AI
- Annual leave

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Project Specialist - Clinical Registry Coordinator - UK Based

IQVIA -
Reading

Apply Now

Job details

Full-time
8 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.

Apply Now

Refine Your Search

clinical research specialist jobs in west byfleet, sry

Project Specialist - Clinical Registry Coordinator - UK Based

Mindworks Hub Clinical Practitioner

Specialist Pharmacy Technician – Clinical Trials

Clinical Trials Assistant

Senior Clinical Scientist (Magnetic Resonance Physics)

Research Assistant

Psychological Therapist - Cognitive Behavioural Therapy (CBT)

Clinical Trials Coordinator

Clinical Trials Coordinator part time 0.5 FTE

Medical Information Specialist - US Hours

Analyst - Health Technology Assessment and Outcomes Research (Fixed Term for 1 year)

Research Regulatory Facilitator

Specialist Clinical Coder

Information, Knowledge, and Support Adviser (Rare Dementia Support)

Behaviour Support Practitioner

Clinical Scientist/Clinical Scientist - Graduate Trainee

Mental Health Therapeutic Practitioner

Clinical Physiologist (Neurophysiology)

Clinical Research Fellow

Medical Doctor (UK) - Freelance AI Trainer Project

I want to receive the latest job alerts for clinical research specialist in west byfleet, sry

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