Author jobs in BoltonCrear alertas

Clinical trials are high stakes, demanding high standards. Veramed sets this standard by bringing together the sharpest minds in data management, biostatistics and programming, with cutting-edge technology and proven processes. Our globally connected, caring team delivers quality, precision and collaboration, earning trust through consistency and integrity. From rapid-fire project work to long-term partnerships, Veramed brings the right minds to every challenge. We have exciting Immediate contract opportunities available for Senior or Principal level Statistical Programmers in the UK to work with Veramed. Do you have any of the following skillsets? if so, please reached out detailing your experience of any of the below: • In-depth Study Lead experience - Skilled in leading studies and SAS expertise., • R Programming skills - Previous experience of working in R and ability to help deliver training., • Macro Development expertise - In-depth experience in creating, maintaining, and governing Macros. ADDITIONAL REQUIREMENTS: • Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs., • Author and review simple and complex study TFL shells., • Author and review simple and complex dataset standards., • Perform data checks and data exploration (e.g. using frequencies, histograms)., • Program and QC routine and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice., • Complete and review CDISC Validation tool reports., • Ensure the appropriate standards are being applied and adhered to., • Familiarisation with simple statistical techniques (e.g. t-test, ANOVA, regression, standard survival)., • Review of project management related documents., • Maintain study master file documents and any other documents that are required to be audit ready. Please use the link to apply or if you wanted to have a chat feel free to reach out to me at or via LinkedIn.

Clinical trials are high stakes, demanding high standards. Veramed sets this standard by bringing together the sharpest minds in data management, biostatistics and programming, with cutting-edge technology and proven processes. Our globally connected, caring team delivers quality, precision and collaboration, earning trust through consistency and integrity. From rapid-fire project work to long-term partnerships, Veramed brings the right minds to every challenge. We have an exciting opportunity for a Principal or Senior level Statistical Programmer skilled in SAS & R to join us on a permanent basis in the UK. We can offer home and/or office working, training and support and a competitive package. The purpose of the role is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Senior or Principal Programmer may also perform a supervisory role (e.g. line management and/or project management). Key Responsibilities Technical • Previous experience with SAS and R., • Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs, • Author, review and approve study TFL shells and dataset specifications, • Author, validate and document SAS programs for datasets, TFLs and macros, applying good programming practice • Identify data issues and outliers, • Complete, review and approve CDISC Validation tool reports, • Identify data and standards issues and resolve or escalate as appropriate, • Awareness of emerging standards and associated impact to ongoing and future planned trials, • Maintain proficiency in SAS and awareness of developments, • Maintain study master file documents and any other documents that are required to be audit ready General • Lead internal and client study, project and cross functional team meetings effectively, • Present study updates internally and at client meetings, • Share scientific, technical and practical knowledge within the team and with colleagues, • Perform work in full compliance with applicable internal and client policies, procedures, processes and training • Build effective collaborative working relationships with internal and client team members, • Ensure learnings are shared across projects or studies, • Develop and provide internal technical training where appropriate, • Lead process improvement initiatives Minimum Qualification Requirements • BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience), • At least 6 years of relevant industry experience Other Information/ Additional Requirements • Understanding of clinical drug development process, relevant disease areas, endpoints and study designs WHAT TO EXPECT: • A warm, friendly working environment in which to thrive both personally and professionally., • A supportive, open-door management policy that will aid in your development and provide you with the tools to take your career to the next level., • A truly unique CRO that’s doing something different when it comes to managing staff, projects and building relationships in the industry., • The ability to own your role and develop your skills and experience.

Technical Author (Medical Devices / Engineering).

Technical Author (Medical Devices / Engineering) Bury, commutable from: Manchester, Rochdale, Oldham, Failsworth, Bolton, Heywood, Farnworth, Middleton, Prestwich, Ramsbottom, Littleborough & all surrounding areas £40,000 - £45,000 + Bonus + Life Assurance + Excellent Company Benefits

Job Description Technical Author (Medical Devices / Engineering) Bury, commutable from: Manchester, Rochdale, Oldham, Failsworth, Bolton, Heywood, Farnworth, Middleton, Prestwich, Ramsbottom, Littleborough & all surrounding areas £40,000 - £45,000 + Bonus + Life Assurance + Excellent Company Be

A leading defence organization in Bolton is seeking a Technical Author to develop and deliver Technical Publications for a diverse portfolio of products across Air, Land, and Sea domains. The ideal candidate has essential technical authoring experience, familiarity with SGML and S1000D tools, and th

Authoring specialists to support and develop complex engineering descriptive and procedural documentation. Experience in technical authoring is essential. Use in particular of SGML is required but also the ability to adapt to other formats of authorship is desirable.

A healthcare engineering firm based in Limefield is seeking a meticulous Technical Author to produce critical documentation like validation and compliance reports.This role involves preparing manuals and test protocols that ensure products meet industry regulations, crucial for supporting safe patie

Technical Author Location: Hybrid, Office based in Stevenage Salary: £37,000-£42,000, DOE + BenefitsContract: Full Time, Permanent Hours: 37 hours per weekBenefits include: Company Pension scheme Private Medical Insurance Life Assurance 26 days holiday (excluding bank holidays) Employee Assistance

We are looking for a Technician Author for our client Sonovision who is a leading provider of Engineering Support Services to clients.

Our client, a specialised consultancy in the nuclear sector, is currently seeking a Technical Author for a contract position based in Cumbria. Proven experience as a Technical Author or similar role.

A leading engineering firm is looking for an E3S Case Author to develop the Environment, Safety, Security, and Safeguards (E3S) Case for a Small Modular Reactor. The role involves authoring technical documentation, ensuring regulatory compliance, and engaging with stakeholders. Candidates should hav

Technical Author – Defence & Engineering Sector. Take ownership of Technical Publications Support the technical authoring of bid/tender/quote submissions. Applying structured authoring techniques and maintaining consistency across documents.

A leading defense contractor in the United Kingdom seeks a Senior Technical Author to manage technical documentation for the Dreadnought submarine project.

If you’re an experienced Technical Author with experience working on engineering documents and are looking to work for an organisation that puts integrity and people at the forefront of everything it does then submit your CV to apply today. Proven background as a Technical Author, ideally within e

A prominent logistics company in England seeks a Technical Author to create and maintain technical documentation.

The Author Academy gave me a hugely helpful insight into how publishing works and how I might find my place as an aspiring author. Pavan Amara, author of forthcoming Mirror, Mirror (The Borough Press). Our next courses start in May 2026 and run for six weeks, with live-streamed tutorials, author rou

An innovative AI research initiative is looking for established authors to participate in paid research interviews. This unique opportunity allows authors to share their insights on recruitment, technology, and personal development, directly influencing the development of cutting-edge AI learning. C

Candidates should have over 5 years of experience in aerospace documentation and proficiency in authoring tools.

A key player in nuclear technology located in the UK is seeking a Senior E3S Case Author to produce E3S Cases and Safety Analysis Reports. This role involves authoring technical documents, developing Claims, Arguments, and Evidence structures, and engaging with regulators and stakeholders.

You will be responsible for authoring highly technical documentation, ensuring compliance with regulatory requirements, and engaging with internal teams and external stakeholders, including regulators and customers. Author E3S Case and Safety Analysis Report documents in line with governance and qua

Contribute to technical authoring for bids, tenders, and quotations. Previous experience in a Technical Author role. An experienced Technical Author is required to create, update, review, and maintain high-quality Technical Publications for customers in the UK and internationally.

Even the most junior Technical Authors will have the opportunity to develop and demonstrate technical authority. Technical Author (multiple roles and seniority levels). Technical Author (multiple roles and seniority levels).

A leading multicloud solutions provider is seeking an experienced Tender Writer / Technical Author in Greater London.

A prominent defence consultancy in Hampshire is looking for a skilled Technical Author to enhance their technical documentation team.

A leading defense technology firm is seeking a Technical Author to create and maintain clear documentation for complex engineering products.

A leading publishing company in Greater London seeks a Marketing Manager for Open Access and Author Marketing.

A specialist IT and communications company is seeking an IT Technical Author to create and edit technical documents for projects.

A leading company in technical documentation is seeking an experienced Technical Author to manage the creation of manuals and technical publications in the aerospace sector.

If this sounds like an IT Technical Author or Technical Draughtsperson role you will LOVE, please send your CV today. Do you have experience as an IT Technical Author or IT Draughtsperson within a technical communications, IT implementation or cyber security environment? Are you looking for an excel

The Senior Author is responsible for managing the end‑to‑end quality process, from storyboard development to final submission of allocated questions, with support from a Lead Author, ensuring all outputs are high‑quality, compliant and compelling. Work collaboratively with Lead Author, Senior

Technical Authority - Romsey Based. Copello are working with a defence & security company who are looking for a Technical Author to join the team. Support the technical authoring of bid/tender/quote submissions.

Support Senior Authors, Authors and Question Owners in strategically translating the value proposition into high‑quality written responses. Actively support senior authors and authors to illustrate “what good looks like” in submissions. The Lead Author is responsible for managing a team of aut

Technical Author and on‑site Publications team in:. Technical Publications team in the required authored content and supporting illustrations.

Depending on the experience of the author, both author and senior author roles are available. Technical Author page is loaded## Technical Authorlocations: Loudwater, Buckinghamshire, England, UK: Greenford, Greater London, England, UK: Weymouth, Dorset, England, UKtime type: Full timeposted

This role would suit anyone with the following job titles - Technical Author, Engineering Documentation specialist, Documentation Engineer, Technical Editor or anyone with similar experience. Experience with structured authoring tools and illustration software is advantageous.

An established online retailer is seeking a skilled Technical Author to enhance customer experience through precise product specifications.

A leading provider of Technical Publications in the UK is looking for a Technical Author to produce S1000D data modules for the Nuclear Sector.

A leading engineering firm is looking for a Senior E3S Case Author to create safety analysis reports and E3S cases, ensuring regulatory compliance.

We have an exciting opportunity for a.IT team based in the A&O Shearman.The core of the global technology department's mission is to provide stable, reliable, and secure platforms and services to our partners, staff and clients and fulfil our regulatory obligations across 30+ countries.To ensure tha

A leading freelance marketplace is looking for a Freelance Marketing expert to provide remote mentorship to authors seeking to expand their audience. This role offers a flexible work arrangement while making a direct impact on authors' marketing success.

A defence and security company is seeking a Technical Author based in Romsey. Candidates should possess a degree or HND/HNC and previous experience in technical authoring, alongside knowledge of relevant standards such as JSPs and S1000D.

A leading infrastructure solutions firm in the UK is seeking a skilled Lead Author to oversee bid submissions and ensure high-quality outputs. Responsibilities include managing the authoring team, ensuring quality assurance, and engaging with stakeholders.

The Author Academy gave me a hugely helpful insight into how publishing works and how I might find my place as an aspiring author. Budding authors can apply for one of the Academy’s limited 45 places, split into three live teaching streams as shown below:. If you believe there’s an audience for

Authoring and managing DMs in the EAGLE Publishing System (EPS) Common Source Database (CSDB) using the EPS xml Editor software.

Experience of Training and Technical Authoring to challenging timescales. As a Technical Author within the Systems Delivery Team, you will liaise closely with several departments both in the UK and globally. Produce high-quality Training and Technical Publications in compliance with relevant standar

A leading defense technology company seeks a Technical Author to create and maintain clear technical documentation for innovative engineering products.

E3S Case Author page is loaded## E3S Case Authorlocations: Manchester, UK: Warrington, UK: Derby, UKtime type: Full timeposted on: Posted Todayjob requisition id: JR100613E3S Case AuthorLocation: Derby | Manchester | Warrington | Other UK LocationsDepartment: Safety & Regulat