Scientific and QA jobs in Reading

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 - Vendor Management Expert to join our Single Sponsor Department . In this role, you 'll become an expert in Vendor Management for global clinical trials across all phases (Phase I-IV), ensuring seamless execution from study start-up through close-out. What We're Loo…

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 programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses. Main Responsibilities and Accountabilities: Collaborates with the study teams to design data structure and specifi…

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 coordinating the development of integrated programming solutions, serving the full spectrum of statistical programming needs. You will provide internal consulting services, including specifications and user needs analysis for complex project…

Starting off on days for training this will move to a shift pattern which is a mixture of DAYS and NIGHTS, working from Monday to Thursday depending on business needs. 6.30am starts, so must be able to reach Reading for early starts. This is an administrative role providing daily support to the Lab Team in Chemistry Lab and the Quality Department. We are looking for a self-motivated individual who is able to follow standard work processes unaided. The successful candidate possesses a high level…

Stantec's Environmental Team is working closely with our water clients to develop innovative, sustainable, and efficient solutions to their needs by applying genuinely new ways of working. We are seeking driven individuals who think differently and love to challenge conventional thinking to join us in a growing, collaborative team of like-minded consultants working to meet the unprecedented industry-wide challenges of efficiency and environmental sustainability. We are currently seeking a Senio…

Overview IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. IQVIA has two teams focused exclusively on amplifying the patient's voice and enhancing their experiences across their health journey: the Patient-Centered Solutions and Connected Technologies (PACT) team, and the Instrument Licensing Solutions and Patient and Site Strategy (ILS & PASS) team. These teams work closely together to generate patient experi…

Your new companyAre you an experienced Regulatory Affairs professional looking to take ownership of life cycle strategy across a dynamic EU portfolio? We're partnering with a leading healthcare organisation to find a Regulatory Affairs Consultant, life cycle management, to join their growing team. This is a fantastic opportunity to play a key strategic and operational role across product life cycle management, working at the intersection of CMC, regulatory strategy, and cross-functional collabo…

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, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward. The Instrument Development and Thought Leadership Segment Instrument Development: This team is responsibl…

The CPM is responsible for execution of trial/program project management deliverables related to budgets and timelines. Evolution of CTOL and Program Coordinator. This position will primarily support the Global Program Leaders (GPLs) in management of a Clinical Team to meet the agreed upon deliverables as outlined in the Compound Development Plan (CDP). Services include understanding the drug development process to deliver a clinical program according to quality, timelines, and budget in close …

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 Review of straightforward medical writing deliverables. Negotiates timelines and discusses/resolves customer comments. Provides written and verbal feedback to junior staff, and to customers when appropriate. Keeps abreast of current medical and/or technic…

The Senior Manager, Biosamples Operations Lead will own end-to-end biosample operations across assigned studies/programs - from operational feasibility, vendor selection, and execution of biosample operations activities through analysis and data delivery. As the primary point of contact for the Study Team on all biosample operations activities, including biomarker and bioanalytical operational activities, you will ensure every biosample is collected, processed, and delivered to the highest qual…

The Senior Manager, Biosamples Operations Lead will own end-to-end biosample operations across assigned studies/programs - from operational feasibility, vendor selection, and execution of biosample operations activities through analysis and data delivery. As the primary point of contact for the Study Team on all biosample operations activities, including biomarker and bioanalytical operational activities, you will ensure every biosample is collected, processed, and delivered to the highest qual…

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 - allowing us to match you with the best-fit project and client environment for your experience and interests IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global cli…