艾昆纬社招岗位

Essential Functions • Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (

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Job Overview Responsible for management and service delivery excellence for assigned projects, covering single or multiple Lifecycle Safety functions (clinical

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Responsibilities Lead study strategy development Partner with Sales, Medical, and Operations teams to develop competitive and operationally feasible solutions

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Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a compl

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Essential Functions • Manage medium scale projects crossing OES core services, functional groups, and regions ensuring high quality deliverable generation posi

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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

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Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulati

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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

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Responsibilities: Supports country SSU strategy in close collaboration with SSO Study Start-Up Team Lead and SSO Study Start-Up Managers to ensure SSU timeline

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Job Overview Serve in support level capacity in CDM Validation (Testing) team, to perform testing activities in CDMS environment to provide efficient, quality

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Job Overview The Global Alliance Management role is responsible for leading and strengthening strategic partnerships with key accounts, ensuring long-term valu

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• 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 del

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Job Overview Provide project related support; assist with designing, loading, and validation of Lab databases using Clinical Trials Management System(s); ensur

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Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard

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Essential Functions • Perform assigned complex administrative tasks to support team members with project execution • Assist in updating and maintaining comple

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Job Overview Work performed is in accordance with ICH E6 Guideline for Good Clinical Practice. Essential Functions • Collect all deliveries from loading bay,

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Clinical Trial Psych Rater - Mandarin Speaking Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Specialist About IQVIA IQVIA

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Role Overview The Global Client Partner is a senior client leadership role responsible for helping Asia-based Emerging Biopharma companies, particularly China-

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requests and studies, including oversight of technical processes and procedures insofar as they impact pathology interpretations. Perform microscopic analyses o

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Job Overview Responsible for performing a variety of technical procedures and experimental execution in support of sample analysis and validation. Responsible

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Job Overview Support the continuous improvement of the staffing function through development and implementation for all staffing programs in an assigned busine

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Essential Functions： Medical Monitoring: Primarily serves as Regional Medical Advisor on assigned projects. Serves as Scientific Advisor and provides guidanc

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Job Overview Develop statistical methods sections of protocols and review case report forms (CRFs). Prepare analysis plans and write specifications for analysi

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Essential Functions • Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (

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Job Overview Under moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regu

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Job Overview Acts as Lead Medical Writer on more advanced writing projects (e.g. complex clinical study reports, protocols, more challenging indications, or cu

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Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions

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背景要求： 1. 满足以下任意要求： 1年以上CRC/CTA/SSU工作经验； 5个月以上CRA经验; 2. 本科及以上学历 3. 英语听说读写流利 职位优势： 系统化培训：4周全脱产培训，快速提升专业能力 薪酬福利：具有市场竞争力的薪资，完善的福利体系 完善保障：五险一金 + 补充商业医疗保险 休

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Create and maintain PO Estimator (POE) calculation. • Manage PO creation, maintenance and closure. • Create, maintain, and close-out site-specific purchase re

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职责 • 准备和组织各种临床研究方案的研讨活动，并与主要研究者或者该治疗领域的专家进行密切 的沟通有关研究方案的事宜； • 根据公司SOP及客户的要求，负责临床研究项目相关的医学撰写工作，如临床研究方案及临床 研究总结报告等的撰写。 • 负责项目的医学审阅工作，如审阅研究方案、知情同意书、研究者手册、和/或病例报

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