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Capital of the UK, home to the Big Ben, the British Museum and Buckingham Palace, London is one of the most famous cities in the world. With more than 2000 years of history behind it, London is filled bursting with iconic buildings, bridges and people.
With more than 170 museums, and over 300 languages spoken by its residents, London is known for being one of the most culturally diverse cities in the world. The British Museum alone contains more than 13million artefacts from the ancient world. If that’s not enough, there is also the National Gallery, the Tate Modern, the Natural History Museum and the Southbank Centre to explore – many of which are free entry, with reasonable admin charges for special exhibitions and events.
London may not be the largest city in the world, but it makes the most of the space it does have - Hyde Park alone offers everything from free yoga to fully fledged music festivals. Whether you want to wander through Camden Market, see Shakespeare’s Globe or catch a Clipper across the Thames… you’ll be hard pressed to run out of things to do - from street food to fine dining, the West End to the IMAX, London has a plethora of *activities to suit any budget.
London is constantly evolving – illustrated by its ever-changing skyline – and the
London job market is booming. In addition to being one of the world’s most significant financial and cultural capitals, London has one of the largest concentrations of universities and higher education institutions in the world – nurturing our future workforce.
Director jobs
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Associate Director, Regulatory Affairs
Permanent / London, England
Job title: Associate Director, Regulatory Affairs A global pharmaceutical business in London is seeking an Associate Director to join their team. This role will be responsible for handling all regulatory activities for phase one and two clinical trials. The ideal candidate will have significant early-stage clinical development experience as well as the ability to communicate effectively across the business. Responsibilities: Define and develop regulatory strategies for projects, particularly focussing on early development up to clinical proof of concept. Lead planning, preparation, and submission of regulatory submissions for EU for example Clinical Trials Authorisations, Orphan Drug Designations, and Paediatric Investigations Plans. Lead communications with EU Health Authorities, including scientific advice meetings with EMA and/or EU Competent Authorities. To maintain detailed working knowledge of the regulatory environment, through direct and indirect contact and relationship with agencies and industry groups. Requirements: Extensive regulatory experience within the pharmaceutical industry, ideally in EU and global regulations. Must have full understanding of the drug development process and where and how regulatory aspects fit into that. An excellent communicator. A life sciences degree would be beneficial. Salary and benefits: A highly competitive salary and wider benefits scheme is on offer To apply for this position or hear further details then please contact Freddie Hill via Freddie.hill@pharma-partners.co.uk
details
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Associate Director, Regulatory Affairs
Permanent / London, England
Job title: Associate Director, Regulatory Affairs A global pharmaceutical business in London is seeking an Associate Director to join their team. This role will be responsible for handling all regulatory activities for phase one and two clinical trials. The ideal candidate will have significant early-stage clinical development experience as well as the ability to communicate effectively across the business. Responsibilities: Define and develop regulatory strategies for projects, particularly focussing on early development up to clinical proof of concept. Lead planning, preparation, and submission of regulatory submissions for EU for example Clinical Trials Authorisations, Orphan Drug Designations, and Paediatric Investigations Plans. Lead communications with EU Health Authorities, including scientific advice meetings with EMA and/or EU Competent Authorities. To maintain detailed working knowledge of the regulatory environment, through direct and indirect contact and relationship with agencies and industry groups. Requirements: Extensive regulatory experience within the pharmaceutical industry, ideally in EU and global regulations. Must have full understanding of the drug development process and where and how regulatory aspects fit into that. An excellent communicator. A life sciences degree would be beneficial. Salary and benefits: A highly competitive salary and wider benefits scheme is on offer To apply for this position or hear further details then please contact Freddie Hill via Freddie.hill@pharma-partners.co.uk
details