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This is a fully on-site position in Jefferson City, MO Are you ready to accelerate your career in clinical research? Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on resp
Our IQVIA team is seeking to hire an experienced Clinical Trials Feasibility Analyst to join an Advanced Analytics group within the Clinical Data Science department. Join this team dedicated to a Pharmaceutical client, focused on efforts in study feasibility analytics. The ideal
Our MedTech RN Clinical Educators experience a unique opportunity to employ their clinical nursing expertise in a new way outside patient care, while continuing to collaborate with healthcare professionals and advocate for the well-being of patients through medical device technol
Join Us on Our Journey to Reimagine Healthcare We are now looking for a Pharmacovigilance Specialist to join our Greek organization. Role Overview The role is responsible for ensuring full compliance with pharmacovigilance (PhV) and product quality processes, acting as a key i
Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Qualifications • High School Diploma or equivalent Req • 3 years administra
Een afwisselende job in het veld, veel autonomie en ruimte om je enthousiasme te tonen? Ontdek jouw volgende uitdaging als medisch vertegenwoordiger. Regio Waasland: Antwerpen L.O., Edegem, Wilrijk, Dendermonde, St Niklaas, Beveren, Puurs, Lokeren. - Je bezoekt huisartsen en sp
Ben jij klaar om elke dag impact te maken in de wereld van diergezondheid en apothekers te inspireren met jouw expertise? - Je bouwt warme, waardevolle relaties op met apothekers en maakt hen enthousiast over een sterk portfolio van antiparasitaire producten. - Je zet elke dag j
- Performing site selection, initiation, monitoring and close-out visits after completing training period - Supporting the development of a subject recruitment plan - Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Cli
Step into a dynamic role where you’ll drive innovation and excellence in clinical research. As a key player in our team, you’ll ensure that study sites are not just compliant but thriving, contributing to groundbreaking advancements in healthcare. When you join IQVIA New Zealand
We are seeking Director, Test Code Product & Lifecycle to join IQVIA Laboratories at Valencia, CA. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we tran
Site Enrollment and Engagement Leads collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The role as a strategic partner to both external and internal stakeholders to optimize the site experience and perform
学历：本科及以上 出勤：每周至少3天 工作地点：北京办公室 工作内容：项目资料的PDF 处理，资料数据核对，以及项目文件清单等的梳理 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We cr
e are seeking a Senior Global Trial Manager to join our team! We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and dev
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, management, and customers. Provide consultation in interpretation of regulat
Are you an experienced mental health professional with clinical trial experience and expertise in psychiatric assessments? We are expanding our global network of Central Independent Raters (CIRs) to support a depression study. ✅ Flexible Working Hours (around 10h per week requi
IQVIA’s Speaker Bureau team consists of dedicated meeting professionals who plan and manage highly compliant meetings and events for Life Sciences organizations. We work with our clients to deliver a high-quality attendee experience through a range of in-person, hybrid, and virtu
Job Overview Develop the local contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements. Qualifications • Bachelor's Degree Related field •
¡Únete a nosotros en nuestro emocionante trayecto! IQVIA ™ es The Human Data Science Company ™, enfocada en el uso de datos y ciencia para ayudar a los clientes de la salud a encontrar mejores soluciones para sus pacientes. Formada a partir de la fusión de IMS Health y Quintiles,
【岗位职责】 支持参与医学事务解决方案（医学策略、医学教育活动、组织运营优化等）相关项目，包括： 1. 案头研究、数据收集、分析和整理 2. 一手调研资料整理&分析，包括访谈纪要整理等，并挖掘insight 3. 协助完成报告撰写，包括PPT的内容调整，版式的设计和修订，翻译等 4. 其他团队交予的工作 【任职要求】 1. 学术背景：国内或海外知名院校的在读本科/研究生，药学/临床等相关背
The Role You will be responsible for coordinating and managing linguistic validation and eCOA projects from start to completion in accordance with IQVIA SOPs. - Managing multiple translation and localization projects at any one time from receipt to completion - Coordinate al