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Manchester (3 days onsite per week).The successful candidate will be responsible for the development and management of technical publications in line with industry standards, with a focus on S1000D and 2000M compliance.This role will involve working closely with engineering, logistics, and support t

Immediate contract opportunities available for Senior or Principal level Statistical Programmers in the UK to work alongside Veramed. Do you have any of the following skillsets? if so, please reached out detailing your experience: • PK Programming expertise - strong NONMEM and Pop PK expertise, • Disclosure & Anonymisation - knowledge and awareness of disclosure and/or anonymisation with experience programming in support of clinical trial disclosures (ex. Preparing uploads to clintrial.gov, etc.). Uses CSR data and tables to prepare. Experience applying data anonymisation rules to study data., • ISS/ISE experience - hands on experience ISS/ISE data pooling. 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.

Veramed prides itself on two key areas: providing the highest quality statistics and programming consultancy for its clients, and giving its employees an industry leading working environment with support and training for career growth. We have an exciting opportunity for a Principal level Statistical Programmer 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 The job tasks listed below outline the scope of the position. The application of these tasks may vary, based on current business needs. Technical • 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 People Management • Line management of statisticians, programmers and other technical staff. Accountable for overall performance of direct reports • Provide coaching and mentoring of staff to achieve “excellence”. Direct employee career development and ensure line reports receive appropriate training to perform their day-to-day jobs • Interview and effectively on-board and integrate new staff members, • Provide programming technical leadership and coaching Project Management • Oversight of key client projects/portfolios. To include: • Being Veramed Project Manager on client accounts and projects, • Maintain the project plan, • Proactive management of resource, scope change and risks, • Manage the delivery of projects to budget, • Manage client expectations and issue resolution 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.

We are seeking suitably qualified Associate or Associate Director Landscape Architect & Landscape Planners with a diverse track record to join our Manchester Landscape & Urban Design team. As a Landscape Planner you would lead, author and co-ordinate Landscape and Visual Impact Appraisals and Assess

Our Environment Group has been providing environmental solutions for our clients for over 30 years in the UK. Deliver and author geo-environmental desk-based studies (preliminary environmental risk assessments) and general quantitative risk assessments to a high standard. Senior Environmental Consul

We’re looking for a Technical Author to take ownership of documentation and drive improvements across a pioneering high-tech engineering company.

An established engineering organisation with a strong track record of delivering complex automation and materials handling projects is seeking a skilled Technical Author. The Technical Author will be responsible for producing professional, client-ready documentation to support the design, delivery,

Exciting Opportunity for a Technical Author in the Renewable Energy Sector! On behalf of our client a global leader in offshore wind energy – we are looking for an experienced Technical Author to support the expansion of the Safe Systems of Work (SSOW) programme across their UK West offshore

An established engineering organisation with a strong track record of delivering complex automation and materials handling projects is seeking a skilled Technical Author. The Technical Author will be responsible for producing professional, client-ready documentation to support the design, delivery,

Providing extensive technical knowledge especially in the area of SDS authoring, undertaking authoring work using Ricardo’s 3rd party SDS authoring software. Extensive background in supply regulations (and potentially transport regs as well); safety data sheet authoring, understanding how to class

As we continue to transition to a digital environment, we know that it's essential to revisit and update our approaches to assessment delivery.Our aim is to create a more modern assessment delivery system that sets us up for the future, supports our Senior Associates better in their role by building

Author / Writer (German language).

Our client, a global leader in advanced technology solutions, is seeking a skilled Technical Author to join their team at a cutting-edge facility in Severn Beach, Bristol.

The CAD Author will be responsible for:. Our OEM Client based in Gaydon, is searching for a CAD Author to join their team, Inside IR35. We are seeking a highly motivated and detail-oriented CAD Author to join the Virtual Build & Test team within Engineering Operations.

We are seeking a highly motivated and detail-oriented CAD Author to join the Virtual Build & Test team within Engineering Operations. The CAD Author will be responsible for:. Our OEM Client based in Gaydon, is searching for a CAD Author to join their team, Inside IR35.

Author sections of NEC4 contract scope documentation in support of procurement events.