Clinical research specialist Work, Jobs in Three Rivers, Hrt (with Salaries)

Project Specialist - Clinical Registry Coordinator - UK Based
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Work from home
11d
Clinical Evaluation Specialist
Scarlet —London
- £75,000 - £90,000 a year
- Full-time
- Nursing
- Sales
- Patient care
Research Regulatory Facilitator
Imperial College London —White City
- £48,246 - £58,318 a year
- Full-time
- Administrative experience
- University
- Time management
- Annual leave
3d
Specialist Clinical Coder
Guy's and St Thomas' NHS Foundation Trust —London
- £47,951 - £56,863 a year
- Full-time
- Hybrid work
- Mentoring
13d
Forensic or Clinical Registered Psychologist - Psychology Services - South West & South Central
Ministry of Justice —Aylesbury
- £50,001 - £60,000 a year
- Part-time
- Hybrid work
- English
- Research
- Supervising experience
- Annual leave
7d
Clinical Research Scientist
Montu UK —Winnersh
- £60,000 - £65,000 a year
- Part-time
- Hybrid work
- Analysis skills
- Project management
- Organisational skills
Quick apply
Specialist Speech and Language Therapist – Adult Neurosciences
University College London Hospitals NHS Foundation Trust —London
- £47,951 - £56,863 a year
- Part-time
- Research
- Patient care
- Communication skills
7d
Medical Doctor (UK) - Freelance AI Trainer Project
Meridial —London
- £40 - £120 an hour
- Remote
- AI
- Annual leave
Clinical Research Fellow Hepatology Medicine
Chelsea and Westminster Hospital NHS Foundation Trust —London
- £49,909 - £61,825 a year
- Full-time
9d
Medical Information Specialist - Afterhours
EVERSANA —London
- Weekend availability
- Remote
- Microsoft Word
- Computer literacy
- English
Quick apply
6d
Corporate Health & Wellbeing Coordinator
HCA Healthcare UK —London
- £31,000 - £41,000 a year
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Employee discount
3d
Medical Information Specialist - US Hours
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- English
Quick apply
Specialist Tutors & Mentors
A Space To Thrive Ltd —London
- £38 - £43 an hour
- Full-time
- Hybrid work
- University
- Bachelor's degree
- Mentoring
Quick apply
4d
Data Acquisition Specialist - External Data (Remote - UK)
IQVIA —London
- Full-time
- Remote
- Computer Science
- English
- Bachelor's degree
- Work from home
5d
Band 6 Agile TRU Clinical Research Nurse
Guy's and St Thomas' NHS Foundation Trust —London
- £47,951 - £56,863 a year
- Full-time
- Medication administration
- Hospital
- In-person
- Annual leave
9d
Clinical Specialist
IQVIA —London
- Full-time
- Customer service
- Communication skills
- Life insurance
14d
Analyst - Health Technology Assessment and Outcomes Research (Fixed Term for 1 year)
MSD —London
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- No travel
5d
Specialist Pharmacy Technician – Clinical Trials
Surrey and Borders Partnership NHS Foundation Trust —Chertsey
- £41,957 - £50,387 a year
- Part-time
- Inventory control
- Travel
- Free parking
4d
Clinical Research & Development Facilitator
Guy's and St Thomas' NHS Foundation Trust —London
- £47,951 - £56,863 a year
- Full-time
4d
Clinical Support Specialist - 12 month FTC, Full-Time
hVIVO Services Limited —London
- Overtime
- Customer service
- Administrative experience
- IT
- Annual leave
- Employee assistance programme

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Project Specialist - Clinical Registry Coordinator - UK Based

IQVIA -
Reading

Apply Now

Job details

Full-time
11 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 specialist jobs in three rivers, hrt

Project Specialist - Clinical Registry Coordinator - UK Based

Clinical Evaluation Specialist

Research Regulatory Facilitator

Specialist Clinical Coder

Forensic or Clinical Registered Psychologist - Psychology Services - South West & South Central

Clinical Research Scientist

Specialist Speech and Language Therapist – Adult Neurosciences

Medical Doctor (UK) - Freelance AI Trainer Project

Clinical Research Fellow Hepatology Medicine

Medical Information Specialist - Afterhours

Corporate Health & Wellbeing Coordinator

Medical Information Specialist - US Hours

Specialist Tutors & Mentors

Data Acquisition Specialist - External Data (Remote - UK)

Band 6 Agile TRU Clinical Research Nurse

Clinical Specialist

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

Specialist Pharmacy Technician – Clinical Trials

Clinical Research & Development Facilitator

Clinical Support Specialist - 12 month FTC, Full-Time

I want to receive the latest job alerts for clinical research specialist in three rivers, hrt

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