Essential Functions： Medical Monitoring: Primarily serves as Regional Medical Advisor on assigned projects. Serves as Scientific Advisor and provides guidance to Project Leaders on the medical and scientific aspects of assigned projects. Provides medical support to
Job Overview Develop statistical methods sections of protocols and review case report forms (CRFs). Prepare analysis plans and write specifications for analysis files, tables, and figures. Communicate with clients regarding study protocol or statistical analysis issues
Company Description Do you want to develop your career and make an impact in the fast-growth, fast-moving B2B technology space? At Informa TechTarget, you’ll collaborate and grow alongside some of the industry’s most respected experts. You’ll
Job Title: Principal Clinical Research Physician (PCRP) Job Location: China, homebased Job Overview: The PCRP, is a Medically Qualified person with extensive experience of in a drug development/drug safety environment or medical data review. PCRP independently
Essential Functions • Review Requests For Proposal (RFP). Identify information for proposal text and budget development and work closely with proposal development team to prepare and finalise proposals. • Prepare text and budget for proposals, rebids
sulting in a reduction of experienced scientific capacity within the Immunology team. During the same period, the department will be supporting a significant HPV testing program, requiring approximately 17,460 HPV IgG and cLIA tests between August
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 development, rewarding and disciplining employees, and addressing employee relations issues and
requests and studies, including oversight of technical processes and procedures insofar as they impact pathology interpretations. Perform microscopic analyses of laboratory assays and monitor digitization of slides. Correlate clinical information with pathology findings. Release timely reports
Job Overview Work performed is in accordance with ICH E6 Guideline for Good Clinical Practice. Essential Functions • Collect all deliveries from loading bay, log, QC, receipt in, store and distribute as required • Maintain stock
Clinical Trial Psych Rater - Mandarin Speaking Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin Us as an Associate Manager Clinical Operations - Make an Impact at the Forefront of Innovation The Associate Manager Clinical Operations oversees the daily line management responsibilities of the
Job Overview Responsible for performing routine analysis and laboratory testing procedures. Essential Functions • Responsible for performing and documenting analytical procedures in accordance with SOPs and regulatory guidelines. • Performs routine data analysis to determine if
Key Responsibilities 1. Manage and coordinate day-to-day support activities, independently handle and resolve complex support cases submitted by clinical trial sites; 2. Provide technical support for medical devices and associated applications at clinical trial sites; diagnose
工作内容： 1， HR相关材料（入离职材料、各类申请表格、证明材料）的整理、打印、盖章和寄送 2， HR系统操作 3， 活动和培训海报制作、礼品寄送、现场支持、培训参与人员信息收集 4， HR数据整理 5， 培训资料库整理 招聘需求： 1.本科或硕士学历，CET-4及以上 2.2027届优先，实习最少3个月，每周出勤3-4天。 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
职责 1.协助DM部门日常工作，包括但不仅限于：数据清理、数据库测试、医学编码、正常值范围管理 2.负责将临床试验数据及时、准确地录入到临床试验数据管理系统中。 3.协助接收、管理、打印、扫描数据管理研究文档。 4.完成直线经理分配的其他工作。 最低学历 医学、药学、流行病学、生物学、计算机相关学科本科学历或同等教育背景。 经验要求： 1. 2027年应届毕业生 2. 每周出勤至少3天；； 4. 英语良好，可以胜任英文读写； 5. 细心，对数据管理感兴趣； 6. 熟悉临床试验者尤佳； IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life
• Supports country SSU strategy in close collaboration with the SSO Study Start-Up Team Lead and the SSO Study Start-Up Managers to ensure SSU timelines and deliverables are met according to country commitments • Accountable for
Job Overview Provide support to the Project Manager and related team members by performing routine procedures and tasks associated with the day to day running of projects throughout the entire study lifecycle (e.g. start-up, maintenance and
主要职责 1.根据试验方案、合同规定的工作范围、SOP和GCP的要求，协助CRA在研究中心进行简单的核查工作。 2.协助CRA进行临床研究相关的文件整理工作。 3. 完成直线经理和/或项目经理（PM）分配的其他工作。 任职要求 1.27届及以上在校生本科或硕士，医药相关专业优先，英语四级或以上。 2.表现优异并能够长期实习。 3.对临床研究和CRA有一定的了解。 4.每周可实习3天或以上（周一至周五），要求可尽快入职并能够至少实习3个月或以上。 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections
Responsibilities: Supports country SSU strategy in close collaboration with SSO Study Start-Up Team Lead and SSO Study Start-Up Managers to ensure SSU timelines and deliverables are met according to county commitments. Responsible for accounting and execution
职位概要 作为研究中心研究者团队的成员，在研究中心遵照研究方案、商定的工作范围、GCP、申办者/公 司SOP及其他相关指南和法规的要求，来协调和执行所分配的临床试验。 职责 • 作为研究团队成员，遵照法规要求、商定的工作范围、适用的SOP、工作授权和试验方案，在 研究中心进行工作。 • 协助研究者完成可行性调查问卷和回收问卷。 • 推动研究中心启动工作：协助研究中心筛选访视，协助及时提交文件到伦理委员会进行审批 和试验用药品的发放，协助研究中心启动访视。 • 协助研究者进行受试者筛选和入组研究。 • 得到研究者授权后，根据法规和GCP的要求，协助研究者顺利完成方案要求的随访和步骤：如 制定计划、清点核对药品和其他协调工作。 • 在研究中心协助研究者管理试验用药品、研究物资和实验室样本。 • 在商定的工作范围内，参加研究者会、监查访视、稽查和其他会议。 • 协助研究者归档研究资料，并提交至伦理委员会或其他权威机构。 • 准确地将原始文件中的数据填写到病例报告表，并协助query的解答。 • 推动研究中心关闭：协助研究中心关闭访视、试验用药品和研究资料的回收，以及研究资料 的归档。 • 创建和维护日常工作报告和其他工作文件。 • 根据工作需要，可能需要不定时出差或暂时借调至其他城市。 • 完成分配的其他任务。 所需知识、技能和能力 •