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.
Permanent / London, England
Medical Director - Clinical Development - Cardiology Pharma-Partners is working with a fast-growing Global CRO to help increase the medical expertise of the business in certain key therapeutic specialties. This organisation has expanded organically and has an operational office presence in multiple countries across the globe. A large proportion of the clinical research projects they manage for biotech sponsors are in rare diseases, across different therapy areas, which means their medical leaders are truly involved in high-science and innovation. A Medical Director in this business is involved "top to bottom" activities, and will find you operating in a flatter more agile structure compared to larger CRO environments where decision-making can sometimes be less rapid. Acting as the therapeutic subject matter expert for global and regional clinical trials cross different phases, you will provide on-going medical expertise for: Clinical trial design and site selection Clinical Study Report creation (CSRs) Trial feasibility assessments Management of Medical Information Regulatory document assessment and submission Supporting Business Development teams, staying involved in proposal meetings and sponsor engagement Management of drug safety activities and medical monitoring responsibility Candidate requirements include: Qualified physician (local country registration required) Recognised specialist in Cardiovascular medicine (Board Certified or equivalent) Experience in clinical research in pharmaceutical medicine, either in a CRO environment or pharma/biotech setting Regional and/or global trial management experience Medical monitoring experience and an understanding of global drug safety best practice Ideally experience of providing medical support to business development activities, including bid defence Someone who enjoys a busy and fast-paced role Good experience managing multiple projects and challenges at one time To apply for this position please use the "Easy Apply" option or feel free to send your CV directly to the Pharma-Partners team via email info@pharma-partners.co.uk
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Permanent / London, England
Medical Director - Clinical Development - Neurology Pharma-Partners is working with a fast-growing Global CRO to help increase the medical expertise of the business in certain key therapeutic specialties. This organisation has expanded organically and has an operational office presence in multiple countries across the globe. A large proportion of the clinical research projects they manage for biotech sponsors are in rare diseases, across different therapy areas, which means their medical leaders are truly involved in high-science and innovation. A Medical Director in this business is involved "top to bottom" activities, and will find you operating in a flatter more agile structure compared to larger CRO environments where decision-making can sometimes be less rapid. Acting as the therapeutic subject matter expert for global and regional clinical trials cross different phases, you will provide on-going medical expertise for: Clinical trial design and site selection Clinical Study Report creation (CSRs) Trial feasibility assessments Management of Medical Information Regulatory document assessment and submission Supporting Business Development teams, staying involved in proposal meetings and sponsor engagement Management of drug safety activities and medical monitoring responsibility Candidate requirements include: Qualified physician (local country registration required) Recognised specialist in Neuroscience (Board Certified or equivalent) Experience in clinical research in pharmaceutical medicine, either in a CRO environment or pharma/biotech setting Regional and/or global trial management experience Medical monitoring experience and an understanding of global drug safety best practice Ideally experience of providing medical support to business development activities, including bid defence Someone who enjoys a busy and fast-paced role Good experience managing multiple projects and challenges at one time To apply for this position please use the "Easy Apply" option or feel free to send your CV directly to the Pharma-Partners team via email info@pharma-partners.co.uk
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Permanent / London, England
Job title: Senior Regulatory Affairs Associate A CRO with offices based in London are seeking a Senior Regulatory Affairs Associate to join their global team. You will be working with local and international teams supporting clinical development across a range of therapy areas such as Oncology, Cardiology, Metabolic Disease, and Endocrinology. Responsibilities: Preparation and delivery of regulatory submissions to domestic and international regulatory agencies. Maintain timelines for components of regulatory deliverables. Perform document quality control checks in accordance with established processes. Maintain and train on up-to-date regulatory requirements, guidance and science; and may be responsible for other projects and responsibilities as assigned. Requirements: Bachelor's Degree in a related field; advanced degree highly preferred (M.D., Pharm.D, Ph.D.) Experience of the EMA Paediatric Investigation Procedure and Investigational Brochure would be an advantage. Good Regulatory Affairs experience in the Biotechnology, Pharmaceutical or CRO industries is essential. Knowledge of EU procedure, ODD and Scientific Advice. Salary and benefits: A competitive annual salary and benefits package is on offer. To apply for this position or hear further details then please contact Matt Thomas via matt.thomas@pharma-partners.co.uk
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Permanent / London, England
Medical Science Liaison (MSL) - Oncology - London & South UK Pharma-Partners is working with a small/mid-sized speciality pharma company with expertise in Oncology. Our client is recruiting a Medical Science Liaison to join their field based Medical Affairs team and cover London and the South of England. As an MSL you will be expected to build partnerships and engage with Healthcare Professionals (HCPs) across the designated territory in the communication evidence based scientific insights. You will work across the Oncology portfolio. Key responsibilities: Establish and maintain relationships with Oncology experts across the region Provide scientific expertise and technical support to Key Opinion Leaders (KOLs) Deliver therapeutically aligned scientific presentations to HCPs Provide medical support as part of a cross functional team to relevant clinical development studies Focussing on patient outcomes, develop local guidelines to support the use of the company's Oncology products Ensure adherence to company SOPs and medial compliance Work with office-based colleagues in Medical and Brand teams, as well as other field-based colleagues, to provide scientific support and education for the company's products Candidate Requirements: Educated to higher degree level (MD, MPharm, PhD, MSc) Experience in the UK pharmaceutical industry is essential Therapeutic area expertise in Oncology Experience in external engagement or customer facing roles Effectively assimilate scientific and clinical data to the relevant audience Understanding of the UK healthcare space Salary & Remuneration: Competitive basic annual salary plus a benefits package to include company car and annual bonus To apply for this position please use the "Easy Apply" option or feel free to send your CV directly to the Pharma-Partners team via email info@pharma-partners.co.uk
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Permanent / London, England
Job title: PV Manager, UK & IE A global pharmaceutical business in London are seeking a PV Manager UK & IE. This is a standalone role and will have responsibility for all markets within the UK & IE regions. Responsibilities: To be the UK contact person and local expert in PV by keeping abreast of current best practice and future developments. Notify GPV and update local standard operating procedures (SOPs) with any changes in UK PV legislation or national requirements. Liaise with Pharmacovigilance personnel regarding initial reports of adverse events so that these may be reported in line with statutory requirements. Communicate changes on product SPCs and PILs to external bodies; alert BNF, MIMS, C&D, PJ and UKMI to changes to Product Licences and SPCs, update SPCs and PILs on eMC website, communicate changes to internal customers, maintain the abbreviated prescribing document for promoted products. Review promotional material in line with Code of Practice; review materials for technical accuracy and correct referencing in line with internal SOP, assist with preparation of data for defence of CoP complaints, as required Requirements: Medical, Pharmacy, Nursing or Life Science Degree is essential Significant Pharmacovigilance experience within the pharmaceutical industry Prior line management experience is desirable Salary and benefits: To apply for this position or hear further details then please contact Matt Thomas via matt.thomas@pharma-partners.co.uk
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