IQVIA
Open positions
CRA Line Manager
Essential Functions • Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance and guiding professional…
Clinical Operations Manager
Essential Functions • Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance and guiding professional…
Clinical Supply Support Associate (Contract)
The role of the Clinical Supply Support Associate (CSSA) – Clinical Supply Operations (CSO) is to provide support for Clinical Supply Operations (CSO) in the areas related to the receipt, packaging, labeling,…
Clinical Research Associate (Canada)
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor…
Investigational Drug Services (IDS) Pharmacy Technician, On-Site
The NEXT Oncology team is hiring a licensed IDS Pharmacy Technician to join our well-rounded, cohesive, and supportive team focused on Phase I, Oncology trials. This role offers a steady Monday–Friday schedule with…
Global Study Assoc. Director - Single Sponsor Dedicated
The Global Study Associate Director (GSAD) is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the delivery of clinical studies. The GSAD is…
Experienced Clinical Research Associate (m/w/d), Multi-Sponsor, Germany
Join IQVIA as an Experienced CRA (m/w/d) in our Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety of indications and learn about…
Clinical Research Associate - Sponsor Dedicated
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor…
Senior Clinical Trial Manager (Oncology, Sponsor Dedicated)
Overview Services rendered will adhere to applicable Sponsor SOPs, WIs, policies, codes of Good Clinical Practice (GCP), local regulatory requirements, etc., while serving as a subject matter expert and resource for…
(Senior) Clinical Trial Manager (II), IQVIA Biotech
🚀 Lead Global Clinical Trials That Change Lives IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and…
(Senior) Clinical Project Manager, IQVIA Biotech
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough…
Global Site Activation Manager, Sponsor Dedicated, Slovakia
Site Activation Manager (Global) Sponsor Facing Homebased Job Overview Lead and manage the strategic, operational, and financial delivery of Site Activation activities across assigned studies and regions. This role is…
Clinical Project Manager
Clinical Project Managers are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Clinical Project Manager is an…
Experienced Clinical Research Associate
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…
Clinical Research Coordinator - Boulder, CO
Clinical Research Coordinator - Boulder, CO Work Set-Up: On-site Schedule Weekly Hours: 24 hours/week About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services,…
Senior QA Auditor (GCP Audits) - Certified to Audit Sites in Italy
Overview Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff,…
Clinical Trial Assistant, HYBRID in Wilmington, DE
Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track…
Clinical Research Associate II - MedTech
MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner, IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together, we support innovation from…
Senior/Clinical Research Associate (Client Dedicated)
As you develop your career as a Senior CRA or CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA, we do not believe in a ‘career ceiling.’ You will be…
Local Trial Manager (Sponsor Dedicated)
Internal Job Description Job Overview Associate Project Leads (Local Trial Managers) are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the…