Research program coordinator Work, Jobs in England (with Salaries)

Project Specialist - Clinical Registry Coordinator - UK Based
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Work from home
Project Coordinator, Data Monitoring - Entry Level
Medpace, Inc. —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Bachelor's degree
- Annual leave
- Work from home
Data Coordinator (London, Entry-Level)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- English
- Bachelor's degree
- Annual leave
- Work from home
eClinical Coordinator (London, Entry Level)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Software troubleshooting
- English
- Annual leave
- Work from home
Career Evening at Medpace London - Project Coordinator
Medpace, Inc. —London
- Full-time
- English
- Bachelor's degree
- Organisational skills
- Annual leave
- Work from home
1d
eClinical Coordinator (London)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Software troubleshooting
- English
- Annual leave
- Work from home
Client Research Coordinator
Dexters —London
- £27,000 - £29,000 a year
- Full-time
- CRM software
- Customer service
- Writing skills
- Employee discount
Quick apply
Client Services Coordinator
Complete Coherence Limited —Romsey
- £30,000 - £35,000 a year
- Microsoft Powerpoint
- Microsoft Outlook
- Communication skills
Quick apply
Quality Coordinator
LEAP Legal Software —London
- Full-time
- Hybrid work
- Microsoft Word
- Bachelor's degree
- Continuous improvement
- Annual leave
- Employee assistance programme
Quick apply
Talent Coordinator
Insanity —London
- £28,000 - £30,000 a year
- Full-time
- Hybrid work
- Conflict management
- Organisational skills
- Communication skills
Quick apply
Scientific BD Proposals Coordinator (ADME/PK)
Pharmaron —Hoddesdon
- CRM software
- Master's degree
- Business development
Program & Experience Design Coordinator, Venture Café London
Cambridge Innovation Center —London
- Full-time
- Hybrid work
- English
- Travel
- Café
- Annual leave
- Employee assistance programme
11d
Clinical Trials Coordinator - London
Re:Cognition Health —London
- £34,000 - £38,000 a year
- Microsoft Powerpoint
- Microsoft Word
- Business development
- Annual leave
- Employee assistance programme
Quick apply
23h
New Product Development Coordinator (18-Month Fixed-Term Contract)
Bio-Rad Laboratories —Kidlington
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Doctoral degree
- Free parking
- Work from home
Coordinator, Online Merchandising
Tapestry Inc —London
- Full-time
- Hybrid work
- Computer literacy
- Analysis skills
- Bachelor's degree
- Employee assistance programme
- Employee discount
Client Service Coordinator
BDA —Manchester
- £30,000 - £35,000 a year
- Microsoft Powerpoint
- Marketing
- Salesforce
Quick apply
XLR Executive Coordinator
Bournemouth Airport —Bournemouth
- £13.78 an hour
- Weekend availability
- Customer service
- Computer literacy
- Computer skills
- Free parking
- Employee discount
Clinical Safety Coordinator
Medpace, Inc. —London
- Full-time
- Microsoft Office
- Bachelor's degree
- In-person
- Annual leave
- Work from home
Inventory Coordinator
Thermo Fisher Scientific —Horsham
- Full-time
- Computer literacy
- Continuous improvement
- Computer skills
1d
Training and Quality Coordinator
Cancer Research UK —London
- £28,000 - £32,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Travel
1d

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Project Specialist - Clinical Registry Coordinator - UK Based

IQVIA -
Reading

Apply Now

Job details

Full-time

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

research program coordinator jobs in england

Project Specialist - Clinical Registry Coordinator - UK Based

Project Coordinator, Data Monitoring - Entry Level

Data Coordinator (London, Entry-Level)

eClinical Coordinator (London, Entry Level)

Career Evening at Medpace London - Project Coordinator

eClinical Coordinator (London)

Client Research Coordinator

Client Services Coordinator

Quality Coordinator

Talent Coordinator

Scientific BD Proposals Coordinator (ADME/PK)

Program & Experience Design Coordinator, Venture Café London

Clinical Trials Coordinator - London

New Product Development Coordinator (18-Month Fixed-Term Contract)

Coordinator, Online Merchandising

Client Service Coordinator

XLR Executive Coordinator

Clinical Safety Coordinator

Inventory Coordinator

Training and Quality Coordinator

I want to receive the latest job alerts for research program coordinator in england

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