Job Title: Senior Regulatory Affairs Officer - Promotional & Non-Promotional Materials Review Location: Reading, UK Working Pattern: 3 days onsite in Reading, 2 days remote per week About This Job As Senior Regulatory Officer - Promotional &
Job Overview Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs Senior
Cambridge (England) Senior Clinical Trial Associate to start ASAP! ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation,
Job Overview Collaborate with pre and post award stakeholders to manage the coordination, planning, quality and implementation of Patient Recruitment and Retention operational plans on small/mid size studies. Position may be responsible for the implementation of
Company Description Network Planning Assistant Because you can see how we can be better. Innovate, your way. Supply Chain at Primark Our supply chain team is the backbone of our operational efficiency. Dive into the intricacies
Team Lead, Technical Support About Us At Seequent, we help organisations to understand the underground, giving the confidence to make better decisions faster. We build world-leading technology that is at the forefront of Earth sciences, transforming
At OQC, we’re building quantum computers that will power the next generation of scientific discovery and commercial innovation. Our mission is to put quantum in the hands of humanity and we’re looking for exceptional engineers to
Wood has an opportunity for a Principal Planning Engineer to be assigned to a Prestigious and World Scale Pre-FEED / FEED Project for Saudi Aramco. This is a challenging and diverse role where they will have
Role Summary The Senior Human Resources Director will serve as a strategic HR leader supporting global business units within Global Clinical Development (GCD), R&D Solutions. Based in Europe, this role partners closely with senior executives on
Job overview Are you a Clinical (Project) IRT Manager with a passion for vendor excellence and study startup success? We’re looking for a Vendor Startup Manager (VSM) to join our Single Sponsor Department, dedicated exclusively to
The Senior Statistical Programmer will be responsible for review datasets in submission ready standard format (ADaM), tables, figures, listings and submission packages. This individual will provide expertise in the design, development and quality control process for
Job Summary: This position is responsible for the development of the end to end design of client standards and study specifications that align to the CDISC standards and regulatory agency guidance’s. This position provides this guidance
Expression of Interest – Tank Welders (UK Projects) We’re inviting experienced tank welders to register their interest for upcoming tankage and heavy-industry projects across the UK. If you’re confident welding large industrial tanks, working to tight
AHEAD builds platforms for digital business. By weaving together advances in cloud infrastructure, automation and analytics, and software delivery, we help enterprises deliver on the promise of digital transformation. At AHEAD, we prioritize creating a culture
At a Glance Legrand has an exciting opportunity for a Sr. Applications Engineer to join the Data Center Power and Control Division Starline Team. This is a remote position reporting to Reading, UK. The Sr. Applications
Legrand has an exciting opportunity for a Manufacturing Engineer III to join the Data Center Power and Control Starline Team in Reading, UK. The Manufacturing Engineer – Electrical Power Systems will support and improve Starline’s manufacturing
Who we are: Geotab ® is a global leader in IoT and connected transportation and certified “Great Place to Work.” We are a company of diverse and talented individuals who work together to help businesses grow
ABOUT QUINCE Founded in 2018, Quince was built to challenge the idea that nice things have to cost a lot. Our mission is simple: to make really high quality essentials for really low prices, produced fairly
Job Overview The Clinical FSP Director Quality - Client Dedicated- Regional Clinical Compliance Inspection Lead is responsible for driving proactive risk management, sustained inspection readiness, audit support, and regulatory compliance across clinical trials. The role provides
Data Centre Engineer At OQC, we aren’t just theorising about the future; we’re building it. Born from a philosophy of bold innovation, we’ve successfully transitioned quantum computing from an academic dream into a commercial reality. The