iqvia

Responsibilities Conduct medical review of clinical trial and post-marketing safety data, including adverse events (AEs), adverse drug reactions (ADRs), coding, causality, expectedness, seriousness assessments, and benefit-risk evaluations. Provide medical oversight and review of safety documentatio

工作职责 协助主管处理药品不良反应安全数据，包括：收集和跟踪传入的不良事件（AE）/终点信息、确定传入事件的初始/更新状态、跟踪事件处理完成的时间表等工作。 协助主管管理项目工作流程，包括数据库录入、质量控制活动和药品安全数据报告的生成，准备药品安全提交档案等工作。 其他主管指派的协助任务等。 任职要求 通过日语N2检定，或具备同等程度日语能力；并通过大学英语CET4级或以上。 学历要求为本科及以上，日语专业可，如具备生物、医药相关背景可优先考虑。 能够保证每周至少出勤24-32小时。 实习地点 大连办公室：大连市高新园区腾飞软件园一期西翼10楼 *接受远程和线下实习相结合的方式 顺利通过实习

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 responsible for accelerating site activation to support timely patient enrollment,

The Senior Customer Success Associate serves as a key client support and delivery partner responsible for ensuring the accuracy, quality, and successful execution of measurement projects. This role manages critical project documentation, conducts rigorous quality control and validation processes, de

IQVIA Biotech is a unique division specialising in working with smaller biotech and emerging biopharma clients and as such we have a vibrant, fast-paced working environment. The sector we are in is cutting edge for therapies with un-met medical need. IQVIA Biotech has an exciting position within its

IQVIA Biotech is a unique division specialising in working with smaller biotech and emerging biopharma clients and as such we have a vibrant, fast-paced working environment. The sector we are in is cutting edge for therapies with un-met medical need. IQVIA Biotech has an exciting position within its

IQVIA Biotech is expanding our Clinical Monitoring team and is seeking CRA 2 professionals with a minimum of 1 year of on-site monitoring experience and oncology solid tumor monitoring experience. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of expe

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare fo

Job Summary We are seeking a skilled and proactive .NET Development Lead to join our global engineering team. The ideal candidate will be responsible for developing, reviewing, and maintaining .NET applications while collaborating with cross-functional teams across time zones. This role requires str

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. ✅ 100% Remote ✅ Flexible Working Hours ✅ Freelance Contract What We're Lo

Financial Analyst – Business Operations Support About the Role This role sits within the Global Procurement and Travel & Payment Solutions team and acts as a hybrid between Finance, Operations, and Customer Support. The role serves as a key connector (‘glue’) between global travel programs, payment

** Pour être éligible à ce poste, vous devez résider dans le même pays/la même région commerciale où se trouve l'emploi ** Location: Canada, Télétravail Aperçu du poste Diriger et gérer l’exécution stratégique, opérationnelle et financière des activités requises de mise en activité des sites, y comp

External Job Description Overview: The Site Investigational Product Specialist (SIPS) will serve as a subject matter expert for nursing administration as it relates to the process and procedure of the IPPI (Investigational Product Preparation and Administration Instructions), specific to drug admini

Market Access represents one of the most critical barriers to patients accessing the therapies they need. Health insurers restrict patient access to therapies that carry less value for them, posing an obvious challenge to drug makers. The IQVIA Market Access Strategy Consulting team (formerly known

IQVIA Strategy Consulting is recognized as a global leader in serving the biopharmaceutical industry and is the management consulting arm of IQVIA, a leading provider of information, services and technology for the healthcare industry in 100+ countries. Our teams offer deep expertise and unique meth

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 as a CRA II, you’ll

【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/临床等相关背景优先考虑 2. 实习经验：具备制药行业/医药领域管理咨询相关实习经验的优先考虑 3. 实习时间：每周实习5天优先考虑，需至少保证每周3个全天，能接受加班；需尽快入职，实习总长度至少可以保证3个月 4. 学习

Job OverviewProject Leads 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 Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet

Job OverviewPerform 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. Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU)

Clinical Trial Nurse – Per Diem - Portland, OR Work Set-Up: Local Travel – In-Home Patient Visits Job Type: Per Diem Are you a Registered Nurse looking for a flexible and rewarding opportunity in clinical research? Join IQVIA, a global leader in advancing healthcare, and make a real impact by suppor