Clinical research associates & coordinators Work, Jobs in Harmondsworth, Gtl (with Salaries)

Senior Coordinator
IQVIA —Reading
- Full-time
- Hybrid work
RESEARCH ASSISTANT
THE FETAL MEDICINE FOUNDATION —London
- From £28,500 a year
- Full-time
- Organisational skills
- In-person
- Communication skills
Quick apply
1d
Clinical Trials Coordinator
University College London —London
- £43,981 a year
- Full-time
- Hybrid work
6d
Clinical Research Associate - IQVIA Biotech
IQVIA —Reading
- Full-time
- No degree
- Travel
- Recruiting
Project Specialist - Clinical Registry Coordinator - UK Based
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Work from home
13d
Clinical Trials Coordinator part time 0.5 FTE
University College London —London
- £21,990.50 a year
- Part-time
- Hybrid work
6d
Clinical Research Associate I
Fortrea —Maidenhead
- Full-time
Research Regulatory Facilitator
Imperial College London —White City
- £48,246 - £58,318 a year
- Full-time
- University
- Time management
- Annual leave
5d
Clinical Trial Monitor
University College London —London
- £43,981 - £52,586 a year
- Full-time
- Spanish
- No degree
- Travel
- Annual leave
- Employee assistance programme
7d
Clinical Trial Practitioner / Clinical Research Nurse
Imperial College London —Hammersmith
- £39,959 - £48,117 a year
- Weekend availability
- Travel
- Data entry
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
- Recruiting
Clinical Research Associate II
IQVIA —Reading
- Full-time
- No degree
- Recruiting
Clinical Research Associate - Midlands
MSD —London
- Full-time
- English
- Microsoft Office
- Bachelor's degree
Community Engagement Nurse (Private Practice Work in the Community)
CareForMe —Hounslow
- £30 an hour
- Part-time
- English
- In-person
- Communication skills
Quick apply
Clinical Research Scientist
Montu UK —Winnersh
- £60,000 - £65,000 a year
- Part-time
- Hybrid work
- Analysis skills
- Project management
- Organisational skills
Quick apply
Clinical Research Nurse
Perceptive —London
- Full-time
- Computer literacy
- Communication skills
- Nursing
- Free parking
Manager, Clinical Study Lead
Regeneron —Uxbridge
- Bachelor's degree
- Continuous improvement
- Travel
- Annual leave
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
6d
Clinical Research Nurse - London
IQVIA —London
- Part-time
- Recruiting
Clinical Research Nurse
Central and North West London NHS Foundation Trust —London
- £47,951 - £56,863 a year
- Full-time
- Travel
- Training & development
11d

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clinical research associates & coordinators jobs near harmondsworth, gtl

Senior Coordinator

IQVIA -
Reading

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Job details

Full-time

Qualifications

Clinical research
Project schedule tracking
Project progress tracking
Progress tracking

Full job description

Reading, United Kingdom | Full time | Office-based | R1557351

Business Unit: Global Site Activation

Location: Reading, UK, hybrid working 2-3 days in office

Make an impact on patient health!

IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes.

We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers.

IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication.

We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available

Job Overview

The Senior Site Activation Coordinator will perform tasks at a country/region level associated with site activation activities in accordance withapplicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include feasibility or maintenance activities.

Essential Functions

Under general supervision, perform feasibility,site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.

Prepare site documents, reviewing for completeness and accuracy.

Inform team members of completion of regulatory contractual. and other documents for individual sites.

Distribute completed documents to sites and internal project team members.

Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.

Review, track and follow up the progress, the approval and execution of required documents such as questionaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.

Requirements

2 years’ minimum experience in a healthcare environment supporting clinical trials required.
Exposure to site activation activities preferred, including but not limited to regulatory submissions, site feasibility, site documentation (questionnaires, CDAs, regulatory, ethics, Informed Consent Forms and Investigator Packs), and site budgets and contracts.

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

Office-based

You’ll work primarily from one of our office locations, collaborating closely with colleagues in a dynamic, team-oriented environment. This setting offers access to on-site resources, real-time interaction and opportunities to build strong relationships through in-person work.

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 associates & coordinators jobs in harmondsworth, gtl

Senior Coordinator

RESEARCH ASSISTANT

Clinical Trials Coordinator

Clinical Research Associate - IQVIA Biotech

Project Specialist - Clinical Registry Coordinator - UK Based

Clinical Trials Coordinator part time 0.5 FTE

Clinical Research Associate I

Research Regulatory Facilitator

Clinical Trial Monitor

Clinical Trial Practitioner / Clinical Research Nurse

Senior Clinical Research Associate

Clinical Research Associate II

Clinical Research Associate - Midlands

Community Engagement Nurse (Private Practice Work in the Community)

Clinical Research Scientist

Clinical Research Nurse

Manager, Clinical Study Lead

Specialist Pharmacy Technician – Clinical Trials

Clinical Research Nurse - London

Clinical Research Nurse

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