As the successful Regulatory Affairs Manager you will be joining our client who is a leading provider of pharmaceutical support services, partnering with life science companies to make medicinal products safer and more accessible for the consumer.
We have an exciting opportunity available for an experienced regulatory affairs associate to enter a company with a great R&D pipeline. The role will involve working with class 3 Medical Devices so experience in this area would be beneficial. Experience with Cardiology clinical trials or animal tissues would be ideal however we will consider any applicants with 3 years' experience in Medical Devices or Pharmaceutical experience.
Our client is actively seeking a Regulatory Affairs/ Quality Assurance Specialist to join their global medical devices operation in Germany.
Our client is a global medical devices company with products and services available in over 100 countries around the world.
Project Manager – Regulatory Affairs (NCEs) – Part home based/Greater London My client, a very well-known and respected consultancy, is looking for an experienced Regulatory affairs professional to join their company. This professional will have 5+years working with New Chemical Entities (NCEs) and managing the whole regulatory process through national and EU procedures. ...
Senior Regulatory Affairs Consultant –Regulatory – Home based The company This company is a top 5 global CRO with a large and ever growing consulting arm. This company is global company with over 10,000 employees across all continents. They are a company that help their clients get medicines into the hands of those who need them most. They offer scientific know how, industry expertise and an outstanding environment to learn and grow. ...
Regulatory Affairs Associate Director
Global Pharma - EMEA - Development Projects
Would you like to work for an organisation that is at the forefront of new Pharma products?
Regulatory Professionals are working on behalf of an international Pharmaceutical and Health Care organisation with the intention of successfully recruiting an Associate Director to work from our clients offices in the Buckinghamshire/Berkshire border.
Senior Regulatory Affairs Associate (Clinical Trials)- Berkshire/West London – Great opportunity to join a leading CRO. Amazing exposure! - JOB SUMMARY: i-Pharm Regulatory has a Senior Regulatory Affairs Associate position for a Senior Regulatory Associate. Moving into the leading CRO will allow great exposure into several therapy areas and give good experience of clinical regulations. ...
Regulatory Affairs Manager A great opportunity for a Regulatory Affairs Manager to step into this strategy role for the EU. Work on ensuring clinical trial approvals for one or more of my client’s products as well as marketed approval for medicinal products. ...
Regulatory Affairs Associate - Senior Regulatory Affairs Associate
Buckinghamshire. One of the world largest Pharmaceutical companies in the world are currently working with Regulatory Professionals to successfully secure them a Regulatory Affairs candidate on a permanent basis to be based in their prestigious offices in Buckinghamshire.
EU Regulatory Affairs Manager / Regulatory Affairs Manager - Clinical Trials
Up to £60,000 per annum plus benefits
As the successful EU Regulatory Affairs Manager you will be joining our client who is a leading provider of pharmaceutical support services, partnering with life science companies to make medicinal products safer and more accessible for the consumer.
PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her