Key responsibilities: An Account Manager is an established and core member of the client services team. Depending on the agency, you will be the lead on one client account and assist on another. At an Account Manager level, the role will remain delivery focused and will be responsible for the day to day management and running of accounts and projects. You will focus on the planning, development and implementation of project deliverables inline with client expectations and ABPI guidelines.
At an Account Manager level, you will be expected to mange your time and workload independently and deliver projects on time and inline with allocated budgets. As an experienced member within the team, you will also help to mentor more junior members of the team (account executives and senior account executives).
As you become more senior within the team, individuals will be expected to become more commercially aware and start to business develop within their given clients. As part of this, you may be involved in business pitches.
Previous roles/experience would include: Candidate will usually have at least 2- or 3-years’ experience within Medical Communications. Occasionally individuals may come from a project management/media background, but knowledge of the pharmaceutical industry is essential.
Usually reports into: Account Director or Client Services Director
Sits within this team: Client Services
Qualifications: Bsc or Msc
Salary band: £30,000 - £40,000 Basic Salary, Pension, Annual Leave, Gym membership, Cycle to work scheme
Keywords: Account Manager, Medical Communications, Medcomms, Healthcare Communications, Medical Education, Advertising, Digital, Public Relations, Pharmaceuticals, ABPI, Mentoring
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
Job title: Global Regulatory Affairs Manager - Home Based A world-leading pharmaceutical business with a broad portfolio of innovative and established medicines in respiratory, HIV, immuno-inflammation and oncology are seeking a Global Regulatory Affairs Manager. In this role, you will be the Regulatory lead for a portfolio of exciting and fast-paced marketed products developing and driving global regulatory strategy in Europe, China, Japan, and Emerging Markets. Responsibilities: Development of regulatory strategy(s) and their execution for assigned asset(s) consistent with the strategic activities for the marketed product portfolio. Ensuring the regulatory strategy will deliver the needs of the local region(s), taking in to account the needs of other regions globally Lead regulatory interactions and the review processes Requirements: Recent experience developing regulatory strategies for established products requiring clinical development (e.g. early post-marketing setting, paediatrics, ahead of loss of exclusivity) Experience of all phases of the drug development process in regulatory affairs, with particular emphasis on maintenance and lifecycle management of marketed products, including for projects with little or no precedence. Extensive knowledge of licensing requirements in all major countries in the region and knowledge of other key Agency processes. Salary and benefits: Alongside flexible home working, this role offers a competitive salary and wider benefits package. 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
Job title: Regulatory Submission (Study Start-Up) Manager A global CRO with offices in Central London are seeking a Regulatory Submissions Manager to join their Clinical Operations team. This is an office-based role with flexibility to work from home 2 days per week. Responsibilities: Efficiently manage and successfully execute all aspects of global start-up Perform quality checks on submission documents and site essential documents Prepare and approve informed consent forms Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and Present during bid defenses, general capabilities meetings, and audits. Requirements: Extensive experience in clinical research, preferably with a CRO. Experience may include CRA or project management experience Knowledge and experience of Clinical Trial Applications within Europe Strong oral and written communication skills; and Team oriented approach and strong leadership skills. Salary and benefits: A competitive annual salary and benefits package is on offer with this role. 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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