- Sr SSU & Regulatory Specialist - UK
Do you want to be part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development.
- Billings Specialist - UK
Do you want to work for a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development.
- Medical Affairs Project Manager (Antibiotics/Anti-Infectives) – UK Based Global Role – Excellent Salary
This leading Global pharmaceutical organisation is recognised for its approach to drug research and is looking for a specialist in this therapy area to provide direct support to the Senior Medical Affairs Leader.
- Senior Regulatory Affairs Specialist
Senior Regulatory Affairs Specialist required for post marketing role - a permanent position with a global pharma company. Competitive salary offered.
- Regulatory Affairs Specialist
Regulatory Affairs Specialist for post marketing role with global pharma company required - permanent position with competitive salary and benefits
- Quality Management Specialist – Clinical Technologies – London, UK
Quality Management Specialist – Meet are partnering with a leading Clinical Technologies who pride themselves on offering the best service to their clients. They are recruiting for a Quality Management Specialist to take full ownership of the Quality Management system within this leading Global organization.
- Senior Clinical Trials Specialist - Feasibility
Senior Clinical Trials Specialist - Feasibility
This is a fantastic opportunity to join a leading Contract Research Organisation on a permanent basis at their operations in Middlesex. This company is within the top 5 CROs in the world, boasting a large number of high profile companies as their clients. Due to high volumes of growth they are seeking a Senior Clinical Trials Specialist to focus on feasibility to come on board to execute and deliver all feasibility within the UK and Irelan
- Regulatory Specialist – Orthopaedics – UK
Salary: £30,000 - £40,000
If working in a fast-paced environment with a wide variety of innovative class I to III devices at the forefront of the industry is where you see yourself, get in touch now!
This is a great opportunity within regulatory affairs to join a world leading medical device company based in South East UK. Join an international regulatory affairs and quality team and gain the opportunity to develop your career on the global platform. ...
- Product Specialist - Notified Body - UK
Salary: £50,000 - £60,000
My client are a world leader in the regulatory field and they are looking to expand their ever growing team by bringing on a Product Specialist.
This is an opportunity to work for a world leading notified body as a Product Specialist, who will be specifically working with csoft tissue resorbables. This position will be part home based, which will allow you to maximise your time conducting other equally important responsibilities. ...
- Regulatory affairs submissions specialist - Regulatory Operations and Info Management - UK - London
To apply please send your CV to:firstname.lastname@example.org or call me on 07951 082482