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.
Regulatory Affairs Manager (Clinical Operations) - London
Regulatory Affairs Manager's (Clinical Operations) primary responsibilities will be to lead the establishment of regulatory studies, creation of regulatory documents and development of regulatory strategy to achieve regulatory approvals and clearances worldwide for interventional and non interventional studies
Senior Consultant – 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. Candidates must be eligible to work in the UK. ...
My client, a dynamic company which is globally recognised as an extremely reputable company has an urgent opening for a Regulatory Affairs Manager CTA. The successful candidate will join the EU Regulatory Team based in the UK.
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 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.
Regulatory Affairs Officer - Medical Devices – Midlands
Our client is a medical devices company who manufacture and distribute wound care and surgical tools globally. Due to continued growth, they are presently recruiting for a regulatory affairs officer to join their Midlands office.
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