Editorial Assistant Jobs in UK : 5 job openings

Sift Ltd
Bristol, England, United Kingdom
Company ...
TITAN ENTERTAINMENT GROUP
London, South East England, GB
Editorial Assistant You will be responsible for fulfilling administrative duties on behalf of the editorial department and providing editorial ...
Headline Publishing Group
United Kingdom
Do you know your pop stars from your social media celebs? Your football legends from your rugby greats? Your hygge from your lagom? The Headline ...
University College London
London, South East England, GB
The post of Editorial Assistant sits within the Marcomms team as part of the Directorate of Marketing and Communications. Marketing and Communications at QMUL ...
Argus Media
London
Job Title Editorial Assistant Reporting Relationship Reports to Managing Editor Location London Head Office, Holborn Job Purpose Argus ...
We made a list of jobs from the category "Media & Publishing", which might suit you
ROLAND MOURET
London
We have an exciting opportunity for a highly organised Workroom/Studio Manager to run the day to day of the workroom at our studio in London.Job PurposeManages the Workroom teamResponsible for running the day to day of the Workroom.To manage all freelance and temporary staff employed in the Workroom.Works on the collection through all development to PP stage.Essential FunctionsUnderstands how to access Gerber in the event of needing to access the RM pattern library/archive.All seasonal fabric and trims to be packed away at the close of the season.Maintains stock audit spreadsheets of all workrooms fabrics and components levels in conjunction with Collection Development.Organise weekly fits in conjunction with the Collection Development Assistants.Responsible for liaising with the Technical Manager in order to book in and plan lay plans, costings and the digitising of patterns in accordance with the seasonal deadlines and company critical path.Create a ‘sample pack’ for the factories, Tech Sheet, Fabric, Trims, Pattern, and Noted up Toile. (Gerber Cutter to supply pattern measurements) in conjunction with the Collection Development AssistantsEnsure all new fabrics have fusing suitability tests actioned.Maintain visual ‘work progression boards’, working rails and priority lists, in-conjunction with the Head Pattern Cutter.Responsible for overseeing the Workroom team in the checking, logging, processing and paying of invoices relating to Studio expenses, Rent & Repairs/Renewals and Fit Model Trackers and day to day budgetary expenses.Responsible for maintaining the Studio expenses, Rent & Repairs/Renewals and Fit Model TrackersWorks directly with Designers throughout the development phase of the collection.Manage/book all freelance Creative Pattern Cutters and Machinists.Responsible for trialling all new freelancersOverall responsible for the budget of the Workrooms and work closely with the Head of Collection Development to ensure the budget remains within seasonal targetsOrganise the prioritisation of patterns, cutting and machining to ensure a smooth regular work flow.If you think this sounds like you and that you have the relevant skills and experience, please apply with your CV and covering note.Please also include your salary expectations with your application.No agencies please. If you need to contact us, please contact HR directly.Unfortunately, we cannot sponsor visas for this role. You must live and be able to work in the UK.The Ideal CandidateKnowledge and SkillsPrevious experience in a similar role managing a very busy workroom for a luxury womenswear brand.To have excellent organisational, administration, and prioritisation skills.To have a knowledge of sizing and fitting.To be the ‘go to person’ for all work room matters both day to day and budgetary.Experience in managing a team, interns and freelancers.A passion for fashion and our brand.To have a basic understanding of grading.To have a logical and pro-active approach to problem solving.
ProPharma Group
Richmond, England, United Kingdom
Company DescriptionProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in the United States, United Kingdom, Australia, and Japan, ProPharma Group’s fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today’s dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.Job DescriptionWriting technical responses such as letters or frequently asked questions (FAQs) to be used to answer enquiries received by Medical Information. This may involve updating existing responses or writing new standard responses.Essential Functions Include:1. Medical Information service delivery• Ensuring that any confidential information or personal data related to ProPharma Group and its clients is managed in accordance with Data Privacy regulations as described in ProPharma Group Standard Operating Procedures (SOPs)2. Quality Assurance• Quality checking own work and that of others within the team under guidance to ensure standards are met and maintained.3. GeneralExtensive training, supervision, mentoring and advice will be provided to support the Associate Medical Information Writer in the conduct of the designated responsibilities listed below:• Carrying out comprehensive and accurate literature searches in Medline, or other databases as required, for technical medical information letters or documents.• Preparing medical information letters or related documents such as FAQs using information gathered from literature searches or similar technical information. This may require condensing large amounts of technical data into concise and readable standard documents. • Updating existing written documents, by checking the information within them is still accurate and up to date, and adding new information identified from literature searches in the most appropriate places to ensure readability and technical flow.• Ensuring that all written items are accurate, readable and technically proficient and comply with Professional Information’s SOPs and the requirements of the client as defined in client specific Working Practices.• Maintaining awareness of, and ensuring compliance with, the legal requirements and professional guidelines associated with the provision of medical information within the pharmaceutical and healthcare industries.• Ensuring that the Confidentiality Statement within the Contract of Employment is adhered to at all times in respect of the data and property of ProPharma Group and its clients.• Working in a professional manner at all times with clients, customers, team members and management.Qualifications1. A human life sciences degree.2. Excellent written communication skills.3. Computer literacy.4. Sound planning, prioritising and organisational skills.5. Excellent accuracy and attention to detail.6. Able to work within a team in an open and professional manner.Additional InformationWe are an equal opportunity employer. M/F/D/V***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
£19000 - £26000 pa
Mattinson Partnership
Yorkshire and Humber, West Yorkshire
We are working with a leading multidisciplinary consultancy seeking to appoint an ambitious Assistant Town Planner or Town Planner to join their Leeds Development Management. You will have the opportunity to work as part of a highly experienced team delivering planning solutions for development proposals across a range of sectors including mixed use, residential, commercial, retail, education and health. The successful candidate will have planning experience within either local authority or consultancy. You will have the opportunity to assist on a diverse portfolio of development proposals and be given full support towards achieving MRTPI status. Responsibilities / Accountabilities: * Provide planning support for an array of proposals for both public and private sector clients * Undertake research and site appraisals * Prepare, submit and negotiate planning applications * Assist in applications, appeals and inquiries, as well as developments, plans and promotions * Liaise with clients and contribute to the generation of new work Qualifications / Experience: * Degree in relevant discipline (e.g. Town Planning) * Working towards MRTPI status * Planning experience either within a consultancy, developer or local authority * Knowledge of the local planning market is desirable * Excellent verbal and written communication skills * Full UK driving licence For further information on this or any other related positions do not hesitate to contact Gavin on 0141 375 7955 or Mattinson Partnership brings together recruitment expertise with hands-on experience. Through our knowledge of the industry, we are able to provide a unique and specialist service. We respect the need for absolute confidentiality and offer every assurance that your application will be handled with the highest levels of professionalism. We actively encourage applications from all sectors of the community. For Further Information on the Mattinson Partnership visit www.mattinsonpartnership.com
Pendragon PLC
Nottinghamshire
This is an exciting opportunity to join our growing marketing team as a Social Media Executive, based within our new marketing office in NottinghamYou’ll work closely with the Social Media and Online Community Leader assisting with social media strategies in line with business goals as well as to support the customer journey. As part of a wider content team you will also work alongside the PR and Content Writing Team as well as digital teams and senior leaders within our business to create and deliver content.Working with numerous leading brands across multiple social media channels you will be involved in the development, scheduling and promotion of social media content as well as reporting on the work you have done.With a background in social media, you’ll have demonstrable knowledge and understanding of social media content planning and experience of copywriting, editing and proof reading. You’ll be proficient in the use of social media tools (Facebook, Twitter, YouTube, Instagram, LinkedIn, Snapchat) and have great verbal and written communication skills. You’ll be organised with great analytical skills and the ability to prioritise tasks and meet conflicting deadlines. You’ll be comfortable with building relationships and encouraging links from the media, bloggers and online influencers via social media, telephone and email.This is a fantastic opportunity to join the UK’s leading automotive retailer, specialising in everything from commercial vehicles, volume brands such as Ford and Vauxhall to premium brands such as Ferrari and Rolls-Royce.
Bristol Myers Squibb
Cheshire, United Kingdom
Detailed Position Responsibilities The following responsibilities relate both to the ongoing work to continue the EFPIA effort as well as the additional responsibilities added to support local teams in countries where transparency laws have been enacted: Data Collection, Reporting & Report Submissions: • Gain and maintain ongoing understanding of the EFPIA code and local disclosure laws. • Interact with internal and external stakeholders including third party suppliers/vendors to gather payments or transfers of value (POTV) and samples data and other required information for reporting purposes. • Manage data feeds coming in from internal systems and external vendors which include mitigating errors and exceptions on a predetermined time frame. • Analyze the data for duplicates, compliance concerns and identification of errors, trends or patterns. • Monitors and communicates any errors found on country dashboards to facilitate data corrections. • Implements corrections to data where internal source systems are not able to make corrections. • Manage preparation and submissions of aggregate spend disclosure reports. • Develops and enhances collaborative relationships across Compliance, IT, vendors and business clients. HCP Disputes & Resolution • Manage the disputes & resolution process by partnering with matrix team (e.g. Compliance, Legal, and Commercial) to track and resolve inquiries and disputes from Covered Recipients. • Implement HCP eStatement and user interface. • Create KPI’s, scorecards/dashboards and share points sites to support HCP Disputes & Resolution. Vendor Management • Implement vendor management process to capture and maintain vendor master list to support manual spend process, training and communications. • Provide operational support to local markets to determine responsible parties for submitting data into the manual spend portal. • Collaborate with local markets to ensure consistent messaging to Covered Recipients, BMS Business Units, Field Force, and Vendors/Suppliers. Education + Bachelor’s Degree required + Consistent experience of Business Operations, IT or Process Redesign with experience in execution and roll-out of new or updates to system applications, preferred + Relevant experience of pharmaceutical marketing/sales and/or medical/research operations experience, preferred + Proven ability to present at executive level + Experience in compliance reporting and large data analytical capabilities preferred. + Technical expertise in large database inquiries and reports required. + Data reporting and visualization experience preferred. + Proficient in Microsoft Excel, Access and PowerPoint + Experience using Concur Expense Reporting and/or SAP is a plus Qualifications Matrix Team Experience: Ability to work within a matrix team (IT, Legal, Compliance), including external vendors and customers. Communication skills: Demonstrated ability to communicate and interact with internal and external clients. Ability to develop analytical communications and deliver analyzed information that is clear, concise, and accurate and understood by the audience. Able to create visualization of analyzed results in executive format. Business process/Analytical expertise: Able to understand complex business operations and processes, and analyze data generated to extract information. Able to associate and interpret unmatched data sets to derive meaning and understanding for business purposes. Business knowledge: Fundamental understanding of healthcare industry, reporting legislation, BMS products and organization. Understanding of internal BMS Business, Compliance and related procedures, processes and requirements. Project management skills: Ability to manage projects across diverse matrix teams. Ability to consider and appropriately incorporate diverse perspectives and opinions while facilitating timely problem resolution. We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.
Prime Global
London, GB
It’s a brilliant time to join the team that puts people first.Here at Prime Global our people are the reason for our success. Sharp scientific and creative minds are the driving force behind our growing business, so our top priority is to nurture a working environment where great talent flourishes. A team that cares An agency that will invest in you High-profile work Advancing science and healthcare Reward and recognition Broad horizons…six fantastic reasons to choose Prime Global.The roleAs a Senior Medical Writer you will have an important role in the development and delivery of scientifically accurate content for our clients’ projects, helping to ensure all work is aligned with client objectives and budgetary requirements.The right candidate will be adept at adapting content and style according to client objectives across a variety of target audiences and subject areas, as well as liaising with a range of medical experts. You will keep up-to-date with different therapy areas, good publication practices and other industry guidelines and processes. You will also enjoy mentoring junior writers in all aspects of the business, and reviewing other writers’ projects.The requirements A life sciences degree, ideally combined with a science Master’s or PhD Approximately 3–4 years’ relevant writing experience Previous medical writing experience from a medical communications or pharma environment across a broad range of projects and/or therapy areas Ideally, experience of attending and supporting clients at scientific meetings (congresses, symposia, advisory boards, etc.) Experience of reviewing, proofing and editing other writers’ work Experience of effectively prioritising and managing your own workload Ability to work effectively as part of a team