Regulatory Science and Policy Associate - VIE Contract Location: United Kingdom, Reading Target start date: 01/10/2026 iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged
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 and Quintiles,
Job Level: Senior Director, Drug Development Location: Home-based in Europe Job Overview: Manages a department or small unit.; Provide leadership and advice on the development of optimum strategies for drug development, product lifecycle management and portfolio
Job Overview Responsible to perform spirometry and other Pulmonary function tests overread for records received from trial sites as per study specific requirements and latest ATS/ERS Guidelines . Job Responsibilities: To perform Spirometry/Pulmonary function tests overread
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
Junior Sales Role / Healthcare sales specialist Location: Liverpool and North West IQVIA is currently seeking a sales professional to join our dynamic team. As part of this role, you’ll have the chance to work with
Business Operations Specialist 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, integrity, collaboration, agility, and inclusion are
Job Overview The Medical Director for the Hematology-Oncology Center of Excellence provides strategic medical and scientific subject matter input to IQVIA in this therapeutic area informed by their training, experience and expertise. The activity of the
Job Overview Oversees, supervises and manages the operational aspects of ongoing projects and programs ensuring quality deliverables on time and within budget. Will ensure that all project work is completed in accordance with SOPs, policies and
Compliance & Quality Manager Location: Reading IQVIA are delighted to be partnering with a growing and highly reputable organisation to recruit a Compliance Manager. This is a key, high-impact role offering the opportunity to take ownership
Principal Data Standards Consultant 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, integrity, collaboration, agility, and inclusion
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 most exciting thing
Our client is recruiting a Key Account Manager to shape and direct the use of a specialist product for neurology across the South West of England You need: A proven track record working in secondary care
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 in South East England. Why IQVIA? Career development opportunities to grow
Dysphagia Account Manager Central region - Leicester & Northampton We’re looking for a commercially driven and clinically credible Dysphagia Account Manager to join a high-performing team supporting a life-changing product across key NHS accounts. This is
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 most exciting thing
Job Title: Senior Regulatory Affairs Officer Location: Reading, UK Working Pattern: 3 days onsite in Reading, 2 days remote per week About This Job As Senior Regulatory Officer - Promotional & Non-Promotional Materials Review within our UK
Lead and execute clinical and operation advanced analytics or system improvements Develop novel data science methodologies to generate deep insights from disparate data sources. Provide subject matter expertise to teams in identification and application of the right
Project Assistant, IDEA 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, integrity, collaboration, agility, and inclusion are
IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams