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 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 leadership
At a Glance Legrand has an exciting opportunity for a Quality Technician to join the Starline Team in Reading, UK. This position is operations primary quality support to frontline employees. The Quality Technician is responsible for ensuring all manufacturing
IQVIA is currently recruiting for a highly accountable Key Account Manager to shape and grow the Intravenous Iron landscape in the West Midlands region. The successful Key Account Manager will be responsible for developing their own
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 smaller
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
As a Principal Biostatistician, you will provide end‑to‑end statistical leadership and integration support across Phase II and Phase III studies, working closely with cross‑functional stakeholders in a fast‑paced, global environment. Key Responsibilities • Provide Principal‑level Biostatistics
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
Project Manager, eCOA Location: UK, home based We are seeking a Project Manager to manage delivery of eCOA projects to internal and external clients . Job Overview Validates the project scope, plans and schedules for moderately
The Trial Delivery Leader (TDL) serves as the single point of accountability for trial operational strategy, trial-level budget, quality, and on-time delivery of assigned clinical trials. This role represents the evolution of the Global Trial Leader (GTL),
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates. Why IQVIA? Career development opportunities to grow as we grow AI‑powered
Join us on our exciting journey! IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health
Virtual Key Account Manager – Smoking Cessation Remote / Virtual Role (Part of a National Team Build) IQVIA is recruiting for an experienced Virtual Key Account Manager to support the growth of a leading smoking cessation
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
Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator. This part-time
Business Unit: Global Site Activation Location: Reading, UK, hybrid working 2-3 days in office Make an impact on patient health! IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience,
Job Overview: As a Principal Statistical Programmer you will provide advanced technical expertise to develop process methodology for the department to meet internal and external clients’ needs, across complex projects and studies. This involves planning and
Global Clinical Project Manager - Vendor Management Expert – Single Sponsor Are you an experienced Vendor Management professional looking to make an impact in global clinical trials? We are seeking a Global Clinical Project Manager -
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 SAS