Regulatory specialist Work, Jobs in Guildford, Eng (with Salaries)

Project Specialist - Clinical Registry Coordinator - UK Based
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Work from home
QA Specialist
MedPharm —Guildford
- Full-time
- Master's degree
- Bachelor's degree
- Continuous improvement
Quick apply
Deputy Manager – Primrose Lodge
UK Addiction Treatment Centres —Guildford
- £40,000 a year
- Full-time
- Supervising experience
- Rehabilitation centre
- Budgeting
- Free parking
- Health & wellbeing programme
Quick apply
Medical Device Regulatory Affairs Specialist
Clinica Engineering Medical Solutions Ltd —Reading
- £3,700 - £4,200 a month
- Full-time
- Engineering
- English
- Databases
Quick apply
Head of Quality & Compliance
The Orpheus Centre- SEN College —Godstone
- £41,000 a year
- Full-time
- Hybrid work
- Analysis skills
- Continuous improvement
- Leadership
- Free parking
- Health & wellbeing programme
Quick apply
Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
Medical Underwriting Coordinator
Unum Group —Dorking
- Full-time
- Hybrid work
- Analysis skills
- Continuous improvement
- Organisational skills
2d
Complaints & Resolution Manager
Skylight Psychiatry —Basingstoke
- £40,000 - £45,000 a year
- Full-time
- Hybrid work
- Travel
- Communication skills
- Annual leave
12d
Reablement Team Leader
Surrey County Council —Woking
- From £34,660 a year
- Hybrid work
- Computer literacy
- Team management
- Computer skills
- Annual leave
- Employee assistance programme
13d
Professional Veterinary Affairs Manager UK & Ireland (175066)
Colgate-Palmolive —Surrey
- £70,650 - £78,500 a year
- Doctoral degree
- Sales
- Business development
Senior Quality Compliance Specialist
Thermo Fisher Scientific —Horsham
- Full-time
- Continuous improvement
- In-person
- Communication skills
Biosamples Operations Specialist
UCB —Slough
Clinical Study Specialist
Regeneron —Uxbridge
- Hybrid work
- Bachelor's degree
- SharePoint
- Annual leave
6d
QA Validation Specialist
Thermo Fisher Scientific —Horsham
- Full-time
- Travel
- Communication skills
Care Manager
SureCare Guildford & Woking —Guildford
- £30,000 - £34,000 a year
- Full-time
- Business development
- Analysis skills
- Bachelor's degree
- Free parking
- Paid training
Quick apply
Assistant Environmental Consultant
SOCOTEC UK & Ireland —Reading
- Full-time
- Hybrid work
- Communication skills
- Employee assistance programme
- Employee discount
Quick apply
4d
Site Start-Up Specialist
Fortrea —Maidenhead
- Full-time
- Hybrid work
- Mentoring
- Communication skills
Operational Risk Analyst
Unum Group —Basingstoke
- Full-time
- Hybrid work
- Analysis skills
- Organisational skills
- Financial services
Quality Engineer (FTC)
Sigma Components Limited —Farnborough
- £35,000 - £46,000 a year
- Full-time
- Analysis skills
- Product management
- Quality control
- Free parking
Quick apply
3d
Junior Brand Innovation Manager
SC Johnson Lifestyle Brands —Frimley
- Full-time
- Analysis skills
- Bachelor's degree
- Continuous improvement

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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

regulatory specialist jobs in guildford, eng

Project Specialist - Clinical Registry Coordinator - UK Based

QA Specialist

Deputy Manager – Primrose Lodge

Medical Device Regulatory Affairs Specialist

Head of Quality & Compliance

Senior Regulatory Affairs Specialist

Medical Underwriting Coordinator

Complaints & Resolution Manager

Reablement Team Leader

Professional Veterinary Affairs Manager UK & Ireland (175066)

Senior Quality Compliance Specialist

Biosamples Operations Specialist

Clinical Study Specialist

QA Validation Specialist

Care Manager

Assistant Environmental Consultant

Site Start-Up Specialist

Operational Risk Analyst

Quality Engineer (FTC)

Junior Brand Innovation Manager

I want to receive the latest job alerts for regulatory specialist in guildford, eng

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