Principal Regulatory Consultant - Regulatory Affairs Project Manager
Up to £65,000 per annum plus benefits. This role is purely home based with no office working.
Having won numerous industry awards and acquired many businesses our client has taken the Pharmaceutical industry by storm. Our client has supported all of the top 20 leading biotechnology companies, all of the top 10 largest pharmaceutical companies and nearly all of the 50 best-selling drugs on the market right now.
My client is a global pharmaceutical company, with offices across the globe. They are currently looking for an RA Program manager with a strong clinical knowledge to come and work in the indication of Oncology. You will either have a complex project or a portfolio of projects, leading a team with clinical dossiers (CTA).
My client is a global pharmaceutical company, with offices across the globe. They are currently looking for an Senior RA Program manager with a strong clinical knowledge to come and work in the indication of Oncology. You will either have a complex project or a portfolio of projects, leading a team with clinical dossiers (CTA).
Regulatory Affairs Associate Director \ Senior Regulatory Affairs Manager
Salary:Up to £74,000 per annum plus benefits
15% bonus target (Approx £11,000). Regulatory Professionals is currently working with a global CRO to provide them with a number of Regulatory Affairs professionals with a strong background in submissions. Our client is looking to build a new team due to acquisitions of other businesses and a large pipeline of work.
Fantastic opportunity for a Senior Clinical Operations Manager / Senior Clinical Project Manager looking to progress into an Associate Director level position within Oncology. You will be responsible for all operational aspects of assigned clinical development programs within a high profile and exciting therapeutic group. You will have worked at program level and ideally have leadership skills.
Regulatory Affairs Manager
West London. £45,000 - £60,000 depending on experience
As the successful Senior Regulatory Affairs Officer/ 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.
A global contract research organisation is looking to appoint a Regulatory Affairs Manager for their London operation. This CRO specialises in the provision of clinical and regulatory services to the pharma and biotech industry. This position would suit an individual with a strong background as a CTA and general clinical development regulatory work.
On offer is a superb opportunity to drive forward the services at this premium central London CRO. ...
If you wish to apply for this role send your CV with a covering note to email@example.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options call Matt Greig or Theo Moore, in the UK London office, on +44 (0)207 801 3380.
I am working exclusively in support of an internationally recognized biopharmaceutical company headquartered in Germany who are looking for a GPMD to be the global clinical trial lead across their portfolio. The Clinical Development Unit Head Auto-Immune Diseases is accountable for the functional excellence of the clinical/ medical team.
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