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
To lead Local Study Teams (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international guidelines such as ICH-GCP as well as
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
Business Unit: Global Site Activation Location: UK, homebased, occasional travel to Reading office (monthly) Make an impact on patient health! IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience,
Purpose of the Role The role of the Security Supervisor is to ensure the overall smooth running of the site, including the recruitment and training of all security staff, whilst maintaining at all times a safe
The FTE Medical Writer will serve as an integrated member of the team, delivering medical writing services for the development of clinical documents, including Clinical Trial Reports (CTRs), Trial Design Outlines/Clinical Trial Protocols (TDOs/CTPs) and CTP amendments,
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
Job Overview IQVIA is hiring an Alliance manager to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent pharma company. In this role, the Alliance Manager will be
Job Overview Manage and support team of Data Management professionals to efficiently produce databases that meet customer requirements. Essential Functions • Provide expert review and guidance for production of Data Management deliverables including CRF/e-CRF, database design
This service primarily leads the development of Digital Health Operations deliverables to meet the needs of the study/program and internal stakeholders. The service will be required to provide technical expertise in Digital Health development, specification development and provide subject
Adjudication Project Manager to join ICON’s Full Service Independent DMC and Endpoint Adjudication (IDEA) team. The Adjudication Project Manager is primarily responsible for managing all endpoint adjudication processes for a clinical trial. ICON is a global
Consultant/Health Economist - Evidence Synthesis. UK/Ireland/Spain/Portugal 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,
Your Mission Be the biospecimen champion in global clinical trials! Drive strategy, ensure flawless sample collection and analysis, and guarantee data integrity. Your expertise powers breakthrough science and accelerates life-changing therapies. What Youll Do + Lead
Business Unit: Global Site Activation Location: UK, homebased, occasional travel to Reading office (monthly) Make an impact on patient health! IQVIAs Global Site Activation Team of 2000 employees, drives best in class site and customer experience,
Your new companyAre you an experienced Regulatory Affairs professional looking to take ownership of life cycle strategy across a dynamic EU portfolio? Were partnering with a leading healthcare organisation to find a Regulatory Affairs Consultant, life
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
Job Title: HEOR Manager Location : Reading, UK Working Arrangements: Hybrid - 3 days per week on‑site in Reading and 2 days remote Two Opportunities Available We are recruiting for two HEOR Manager positions in Specialty
Kenvue is currently recruiting for a: Northern Europe Regulatory Affairs Director What we do At Kenvue , we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science,
Business Unit: Global Site Activation Location: Reading, UK, hybrid working 2-3 days in office Make an impact on patient health! IQVIAs Global Site Activation Team of 2000 employees, drives best in class site and customer experience,