clinical research monitor Work, Jobs in london (with Salaries)

Clinical Research Coordinator - London
IQVIA —London
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Access
Fleming Initiative Clinical Research Fellow in Human Infection Challenge
Imperial College London —Hammersmith
- £52,665 - £73,992 a year
- Full-time
- Laboratory experience
- University
- Communication skills
5d
Clinical Research Associate- North West England
MSD —London
- Full-time
- English
- Microsoft Office
- Bachelor's degree
Clinical Research Associate - South East
MSD —London
- Full-time
- English
- Microsoft Office
- Bachelor's degree
Project Finance Analyst (Clinical Research)
WEP Clinical —London
- Full-time
- Hybrid work
- Microsoft Excel
- English
- Microsoft Office
AI Clinical Product Researcher
Odin Vision —London
- £35,000 - £45,000 a year
- Full-time
- Hybrid work
- Engineering
- Bachelor's degree
- Travel
Clinical Research Nurse
Velocity Clinical Research, Inc. —Romford
- £40,000 - £50,000 a year
- Temporary
- Anatomy knowledge
- No experience needed
- Patient care
- Health & wellbeing programme
- Life insurance
Quick apply
6d
Research Assistant / Associate
Imperial College London —South Kensington
- £43,863 - £57,472 a year
- Full-time
- Doctoral degree
- Engineering
- Machine learning
13d
Research Officer
Royal College of Veterinary Surgeons —London
- £35,000 a year
- Full-time
- Master's degree
- Time management
Clinical Trial Associate Manager
Galderma —London
- Hybrid work
- Project management
- Bachelor's degree
- Leadership
Junior Cardiac Physiologist
Guy's and St Thomas' NHS Foundation Trust —London
- £38,488 - £46,852 a year
- Full-time
- Laboratory experience
- Bachelor's degree
4d
Medical Science Liaison
サイネオス・ヘルス —London
- Doctoral degree
- Travel
Director of Participant Strategy & Engagement
Richmond Pharmacology —London
- Full-time
- Bachelor's degree
- Leadership
- Annual leave
Quick apply
Epidemiologist, Internal Medicine, Inflammation & Immunology (FSP Sponsor Dedicated)
IQVIA —London
- Full-time
- Remote
- Doctoral degree
- Master's degree
- Analysis skills
Health Visitor
Lewisham and Greenwich NHS Trust —London
- £39,959 - £48,117 a year
- Part-time
- Care plans
- Communication skills
4h
Senior CAMHS Clinician - AOT
North London NHS Foundation Trust —London
- £55,524 - £62,652 a year
- Part-time
22h
GCP Compliance Manager - Clinical Programs & Trials
Novartis —London
- Full-time
- Hybrid work
- Engineering
- Communication skills
1d
Single Sponsor Payment Specialist _ (clinical payment exp needed), client based near Gatwick_ needed ASAP.
サイネオス・ヘルス —London
- Travel
- Contracts
- Communication skills
12d
MBT Practitioner
South London and Maudsley NHS Foundation Trust —London
- Part-time
- Management
- Care plans
4h
Scientist
UK Health Security Agency —London
- £37,749 - £45,353 a year
- Part-time
- Hybrid work
- Microsoft Excel
- Microsoft Access
- Presentation skills
12d

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Clinical Research Coordinator - London

IQVIA -
London

Apply Now

Job details

Full-time

Qualifications

Microsoft Word
Microsoft Excel
Microsoft Access
Vital signs
Microsoft Outlook
Clinical research
Ophthalmology
Windows
Microsoft Office
Bachelor's degree
Organisational skills
IT

Full job description

London, United Kingdom | Full time | Field-based | R1545300

Clinical Research Coordinator – London (Short-Term Assignment)

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry-leading company? If so, come and join us. IQVIA is currently looking for a Clinical Research Coordinator to support a short-term clinical study.

This is a short-term study assignment (3 months), working 24 hours per week, supporting a site in Hounslow, West London.

As a pivotal member of the site team, you will be involved in a variety of clinical and administrative tasks to support investigators, ensure the smooth running of clinical trials, and assist with the collection of patient data.

Key Responsibilities

Support clinical research studies and maintain a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator
Safeguard the well-being of study participants, act as a patient advocate, and address participant concerns
Maintain up-to-date study documentation, including study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other essential records
Plan and coordinate logistical activities for study procedures in line with the study protocol
Perform clinical study set-up and preparation, including labeling specimen collection tubes and containers, managing inventory of required supplies, and setting up or troubleshooting study equipment
Assist with data entry, data quality checks, and query resolution to ensure protocol compliance and data accuracy
Support study enrollment activities, including recruiting, screening, and orienting participants according to the study protocol
Ensure correct custody and handling of study medication in accordance with site standard operating procedures
Coordinate with study monitors on study-related issues and respond effectively to monitor-initiated queries
Perform and document patient vital signs

Required Skills and Experience

BS/BA in life sciences or equivalent education and/or relevant work experience in a clinical or medical setting (e.g., Clinical Research Coordinator, Research Nurse, Medical Assistant, or similar role)
Ideally an experienced Research Nurse or a highly experienced Clinical Research Coordinator
Experience in pediatric and/or ophthalmology clinical trials is preferred but not essential
Strong knowledge of clinical trials, including departmental, protocol-specific, and study-specific operating procedures, consent forms, and study schedules
Strong IT skills, with proficiency in MS Windows and Microsoft Office applications (Access, Outlook, Excel, Word)
Excellent interpersonal skills with the ability to build and maintain effective working relationships with colleagues, managers, and clients
Strong organizational skills with close attention to detail

#LI-DNP

#LI-HCPN

#LI-CES

#LI-CT1

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.

Apply Now

Refine Your Search

clinical research monitor jobs in london

Clinical Research Coordinator - London

Fleming Initiative Clinical Research Fellow in Human Infection Challenge

Clinical Research Associate- North West England

Clinical Research Associate - South East

Project Finance Analyst (Clinical Research)

AI Clinical Product Researcher

Clinical Research Nurse

Research Assistant / Associate

Research Officer

Clinical Trial Associate Manager

Junior Cardiac Physiologist

Medical Science Liaison

Director of Participant Strategy & Engagement

Epidemiologist, Internal Medicine, Inflammation & Immunology (FSP Sponsor Dedicated)

Health Visitor

Senior CAMHS Clinician - AOT

GCP Compliance Manager - Clinical Programs & Trials

Single Sponsor Payment Specialist _ (clinical payment exp needed), client based near Gatwick_ needed ASAP.

MBT Practitioner

Scientist

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