- Regulatory Affairs Manager \ Project Manager \ Regulatory Submissions Lead
Regulatory Affairs Manager \ Project Manager \ Regulatory Submissions Lead
£50,000 - £65,000 – flexibility for highly experienced candidates
Location: Flexible home working (can be entirely home based) or East Anglia
Are you looking for a flexible company which allows you to be based from home?
Are you interested in working for a forward thinking, innovative company?
- Regulatory Affairs Manager \ Regulatory Affairs Project Manager \ Regulatory Submissions
Regulatory Affairs Manager \ Regulatory Affairs Project Manager \ Regulatory Submissions
Our client is a leading global contract research organisation providing drug discovery, development and lifecycle management services. Their clients and partners include pharmaceutical, biotechnology, medical device, academic and government organisations.
- Regulatory Affairs Manager \ Regulatory Project Manager
Regulatory Affairs Manager \ Regulatory Project Manager
Location: East Anglia / Home Based. £50,000 - £62,000 per annum – flexibility for highly experienced candidates
Our client is a leading global contract research organization providing drug discovery, development and lifecycle management services. Our client has the luxury of working with clients/partners in many different leading organizations.
- Regulatory Manager
Regulatory Affairs Manager - CMCMy client, a very well-known and respected consultancy, is looking for an experienced Regulatory affairs professional to join their company. This professional will have 6+years working in CMC, predominantly in post approval. Candidates must be eligible to work in the UK. ...
- Project Manager, Regulatory Affairs (Post Licensing) - EMEA-116915
PPD is a leading global contract research organization providing drug discovery, development and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. ...
- Principle Consultant Regulatory Affairs
Principle Consultant Regulatory Affairs - IDMPThe companyThis 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
An attractive job opportunity has arisen at a leading multinational pharmaceutical company who are seeking a Regulatory Affairs Associate to work at their UK site in West London. The company employs 100,000 personnel across 150 countries, working across multiple therapy areas including cardiovascular, oncology, and respiratory. This is a 6 month contract role with the possibility of an extension. ...
- Expert in Pediatric Oral Formulation, Switzerland
A fantastic opportunity has arisen for an expert Scientist in Oral Drug Product Formulation Development to join a global leader in the Pharmaceutical industry. You will develop pioneering oral dosage forms for new chemical entities, predominantly for geriatric and pediatric patients. This position is based in Switzerland.
- Senior Regulatory Affairs Consultant - UK/IRE
A leading US biopharmaceutical organisation with a solid commercial portfolio of life saving drugs within a number of therapy areas have a new Senior Regulatory Affairs Consultant job opportunity at their offices in London. The company has a growing pipeline of investigational drugs and approximately 5,000 employees in offices across four continents. This is a 12 month contract role with the possibility of an extension. ...
- EDMS Regulatory Business Systems Specialist- World leading Pharma - Central London
To apply for this EDMS Regulatory Affairs System role please call Julie Cooper on 07951 082482 or send your CV to- firstname.lastname@example.org