Latest Medical Imaging Specialist Jobs

Clinical Trials Supply Chain Manager

Our client, a global pharmaceutical company, is currently looking for a Clinical Trials Supply Chain Manager to join their team in Uxbridge on a full time, 6-month temporary basis (35 hours per week). This role is expected to be worked on a hybrid basis but remote applications will also be...

Park Street People

City of London

Clinical Trials Supply Chain Manager

Our client, a global pharmaceutical company, is currently looking for a Clinical Trials Supply Chain Manager to join their team in Uxbridge on a full time, 6-month temporary basis (35 hours per week). This role is expected to be worked on a hybrid basis but remote applications will also be...

Park Street People

London

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Bristol

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Glasgow

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Sheffield

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Liverpool

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Nottingham

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Manchester

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Newcastle upon Tyne

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

London

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Birmingham

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

Leeds

Regulatory Affairs Associate

🚀 Join Us as a Regulatory Affairs Associate – Chippenham (Hybrid) Location: Chippenham, 2 days a week onsite (Hybrid) Contract: Permanent Are you passionate about healthcare innovation and regulatory excellence? Alliance is looking for a Regulatory Affairs Associate (known internally as a Regulatory Scientist) to join our Global Innovation and...

Alliance Pharmaceuticals Limited

Chippenham

Global Regulatory Affairs Officer - On-Site Edinburgh

A leading healthcare organization is seeking a Regulatory Affairs Officer based in Edinburgh to develop regulatory strategies, manage product license registrations, and ensure compliance with global standards. The role involves preparing regulatory documentation, advising teams, and monitoring compliance, requiring a relevant degree and prior experience in regulatory affairs or compliance...

SRG

Edinburgh

Regulatory Affairs Manager UKIE

Posting InformationField of work: Regulatory & MedicalPosting Date: 11 Nov 2025Application deadline: 24/12/2025Location: Maidenhead SL6 3UD, Berkshire, United KingdomContract type: PermanentJob ID: 3940Shape the LEO Pharma of tomorrowLEO Pharma is looking for an experienced Regulatory Affairs professional to join our UK & Ireland team in a pivotal role ensuring our...

レオ ファーマ株式会社

Maidenhead