Post-Trial Access Manager, Continued Access is accountable for the execution of multiple global PTA programs, of mild and moderate complexity, with minimal supervision. PTA here refers to the provision of investigational product for the intent of
Overview IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. The Patient Centered Solutions (PCS) Strategic & Scientific Research (SSR) team leads the industry in generating
We are seeking a self-motivated Director to lead the development of the EMEA CPM function. This role requires a dynamic leader who thrives in ambiguity, builds high-performing teams from the ground up, and drives alignment across stakeholders.
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 practices.
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
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 You’ll Do Lead Biospecimen
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
Location - Maidenhead Job type - Permanent Hours - 37.5 hours per week, Monday to Friday. Hybrid role, minimum of 3 days in office, 2 days remote. Additional on site attendance may be required to meet
Job Overview (CRAs are encouraged to apply) This role is assigned to designated Delivery Unit(s), sponsor(s), business line(s), and/or specific tasks as defined by the Line Manager (LM). The purpose of this role is to implement
Principal R&D Scientist – ELISA Development BioChek is a global leader in veterinary diagnostics, specialising in advanced ELISA and PCR testing solutions for the animal health industry. With a strong focus on innovation, scientific excellence, and continuous
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
Advertising Performance Manager (APM) Location: Remote / UK-Based Salary: £32,000 - £40,000 depending on experience Company: Amersify About Amersify Amersify is a strategy-first Amazon growth consultancy. We don’t just run campaigns - we help brands understand
Your new company Are you an experienced Regulatory Affairs professional looking to take ownership of lifecycle strategy across a dynamic EMEA portfolio? Were partnering with a leading healthcare organisation to find a Regulatory Affairs Consultant -
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
Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. _Home
The IQVIA Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our clients project team to set-up and execute clinical trials. Senior Clinical Project Support Specialist will provide operational support and coordination
We are seeking a highly motivated Director Clinical Operations to lead the development and implementation of the cFSP Clinical Project Management team . This individual will be a dynamic leader, comfortable working in a fast-paced and ambiguous
NetSuite Developer | Fully Remote - UK BASED ONLY | £50-60k I am working with a NetSuite partner who need a mid-level developer to support implementations and ongoing optimisation across their client base. The work: SuiteScript
Job Overview IQVIA is hiring a clinical project 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 clinical project manager
_Job Overview_ _IQVIA is hiring to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent Pharma company. Associate Clinical Project Managers (aCPM) are an integral part of clinical