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account manager
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
Account Manager jobs
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Interim Product Manager
Contract / Cambridge, Cambridgeshire
Interim Product Manager - General Medicine (12 months - inside IR35) This is a UK based role. Pharma-Partners is working with a well-known global biotechnology business to hire an interim Product Manager. The Product Manager will lead the development & execution of vibrant multi-channel content, make the most of large accounts, & assist in development of strategic & operational plans for core cardiovascular & osteoporosis brands. Key responsibilities: Co-develop general medicine strategic plans & portfolio of activities Manage development of high investment activities Deliver national access plans with the market access lead Develop & deliver omni-channel marketing campaigns in order to maximise customers across all channels Analyse & interpret sales data, KPIs, & market research Lead cross functional teams in developing marketing plans & activities Forge strong relationships with sales heads to ensure salesforce alignment Contribute input into European brand plans Candidate Requirements: Proven pharma/FMCG marketing experience Experience successfully planning & executing marketing initiatives, building customer segments & multi-channel marketing Strong analytical skills ABPI/IPHA codes of practice literate, & familiar with regulatory frameworks Demonstrable leadership skills & ability to work well in a cross functional environment To apply for this position please use the "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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Regulatory Information Management Project Manager
Permanent / Essex, England
Job title: Regulatory Information Management Project Manager A global pharmaceutical business in Essex are seeking a Regulatory Project Manager. This role will focus on Regulatory Information Management in the Global Regulatory Operations team. Responsibilities: Develop and implement the RA business systems strategy required to ensure that Global Regulatory Affairs (GRA) systems continue to meet ongoing and emerging business needs. Provide the expert business analysis input required for the successful development of strategic system roadmaps and for the successful implementation of the projects required to ensure the delivery of the technology solutions required to support the GRA business and its partner functions. Manage and deliver XEVMPD submissions operation to ensure Article 57 compliance. Requirements: Bachelor's Degree in Life Sciences or Information Technology (required) Demonstrable experience of the Pharmaceutical industry with direct experience in Regulatory Affairs Knowledge of global (FDA, EMA, Health Canada and Japan) regulatory requirements. Experience with Parexel (Calyx)/Liquent's Insight regulatory information management suite of products (desired) Knowledge of industry regulatory standards (eCTD, CDISC, EVPRM, SPL, ISO IDMP etc). Salary and benefits: A highly competitive salary, annual bonus, private healthcare and wider 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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Medical Affairs Manager - Pipeline Lead
Permanent / Buckinghamshire, England
Medical Affairs Manager - Pipeline Lead Pharma-Partners is working with a mid-sized specialty pharmaceutical company to hire a Medical Affairs Manager for the UK and Ireland (UK&I) team. This is a strategic role responsible for bringing new drugs to market across the UK&I and will act as the medical lead for a diverse pipeline across Rare Diseases, Oncology, Haematology and Women's Health. As the business continues to bolster the portfolio through new drug acquisition the Medical Affairs Manager will continuously provide expertise to the wider business for new launches, whilst the wider team of Medical Advisors manage the marketed treatments. This position reports directly into the UK & Ireland Medical Director. Key responsibilities: Develop and implement medical strategy for pipeline drugs with a particular focus on launch activities Support the Medical Director in carrying out day-to-day activities of the medical department Input into Global projects Establish and maintain relationships with KOLs Provide medical expertise to the cross functional launch team Support Marketing in the development of the Brand Plan Work closely and collaboratively with Market Access colleagues as required Work with local and global teams on evidence generation plans and IITs Provide internal scientific training where necessary As part of a cross functional team provide medical input into lifecycle management plans Review and approve materials in line with the ABPI Code of Practice Candidate Requirements: UK registered Physician or Pharmacist with Final Signatory status (essential) Several years of UK Medical Affairs experience as a Medical Advisor or equivalent New product launch experience is very beneficial Any therapy area background will be considered Project leadership skills Excellent communication and presenting skills Salary & Remuneration: Competitive basic annual salary plus a benefits package to include car allowance 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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Regulatory Affairs Project Manager - Homebased
Permanent / Buckinghamshire, England
Job title: Regulatory Affairs Project Manager - Home Based A research-oriented pharmaceutical company in Buckinghamshire are seeking a Regulatory Affairs Manager to work across the UK and EU markets. This role will mainly focus on maintenance of marketed products but will also have coverage to work within development assets. Responsibilities: Act as key regulatory contact for interactions with the local authorities on all regulatory matters Submit, maintain and manage regulatory applications/periodic reports and renewals ensuring regulatory compliance Input and prepare relevant sections of Marketing Authorisation, variations and clinical trial application dossiers to gain regulatory authority approvals Provide scientific and technical support, and ensuring the information exchange of regulatory affairs matters, to internal and external stakeholders Requirements: Minimum of 5 years' experience within Regulatory Affairs (Ideally Pharma) Experience within UK/IE and EU markets is essential Full life cycle experience is essential Ability to work with various cross functional teams and departments Salary and benefits: A highly competitive salary, annual bonus and private healthcare are 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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Regulatory Affairs Project Manager - UK/IE
Permanent / Berkshire, England
Job title: Regulatory Affairs Project Manager - UK/IE A Top 10 Pharmaceutical business in Berkshire are seeking a Regulatory Affairs Project Manager. This is a UK/IE affiliate role and will work across an Oncology or Immunology portfolio. Responsibilities: Serves as Health Authority liaison and interfaces with Health Authority Lifecycle management of applicable products and management of Clinical Trial activities with the MHRA Reviews promotional, non-promotional and training materials, as applicable, and ensure the materials are compliant with local regulations and internal policies and procedures. Ensures submission and content of new Marketing Authorisations, variations and other regulatory submissions, including label, artwork and local prescribing information are made in accordance with appropriate timings and requirements and maintain an appropriate tracking of the process as applicable Requirements: Life Sciences Degree or equivalent experience Varied experience within Regulatory Affairs, including commercial affiliate awareness and clinical trial knowledge Experience of reviewing material against the ABPI Code of Practice Therapy experience within Immunology or Oncology would be desirable Salary and benefits: A competitive salary, annual bonus, car allowance and further 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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