远程工作雷达

CRA II 或 SrCRA I(男女均可),单一赞助,居家办公 奥地利

CRA II or SrCRA I (m/w/d), Single Sponsor, home-based Austria

职能支持限定地区(需当地身份)日间重叠约 2 小时,需偶尔早起或晚睡
公司IQVIA
薪资€4,200
工作地点Austria
地域资格限定地区(需当地身份)
时区要求日间重叠约 2 小时,需偶尔早起或晚睡
用工类型Full Time
发布时间今天
数据来源Himalayas
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注意地域限制:该职位明确限定在 Austria 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。
作息提示:日间重叠约 2 小时,需偶尔早起或晚睡。

加入IQVIA,作为临床研究助理II或高级临床研究助理I(男女皆可),在奥地利全境远程工作,任职于我们的单一赞助商部门,开启您的临床研究职业发展。您将享受到一家领先全球的合同研究组织的稳定性和资源,同时直接与我们的客户合作积累经验。无论您是刚刚起步还是希望深化专业知识,这个职位都将带来有意的职业成长和专业发展机会。通过获得世界级的培训和指导,您将在一个旨在帮助您在多种治疗领域积累经验的环境中,发挥您的热情。

您的职责包括:

  • 执行现场选择、启动、监查和结束访问
  • 支持受试者招募计划的制定
  • 根据监管要求(即良好临床实践(GCP)和国际人用药品注册技术协调会议(ICH)指南)评估现场实践的质量和完整性
  • 通过跟踪监管提交、招募、病例报告表(CRF)完成情况和数据查询解决来管理项目进展
  • 与研究现场的专家及客户代表合作
  • 根据客户模式,可能涉及远程监查、参与研究启动流程、专注于治疗领域(药品或医疗器械)
  • 指导经验较少的团队成员,作为特定主题的专家支持,或可能包括其他任务

资格要求:

  • 生命科学或其他科学领域的大学学位,或医疗保健领域的学徒经历
  • 至少两年的现场监查经验
  • 熟悉适用的临床研究监管要求,即良好临床实践(GCP)和国际人用药品注册技术协调会议(ICH)指南
  • 良好的书面和口头沟通能力,注重细节,能够在快节奏环境中工作
  • 德语流利,至少达到C1级别,英语熟练
  • 能够灵活地将工作时间的40-60%用于出差
  • 拥有B类驾照

您将获得:

  • 促进职业发展的资源
  • 支持灵活工作安排的领导
  • 帮助您建立治疗知识的项目
  • 提供新体验的动态工作环境
  • 远程办公,公司车辆
查看英文原文

Join IQVIA as a Clinical Research Associate II or Senior Clinical Research Associate I (m/w/d) home-based throughout Austria in our single sponsor department, and advance your career in clinical research. You’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
Your responsibilities will include:

  • Performing site selection, initiation, monitoring and close-out visits
  • Supporting the development of a subject recruitment plan
  • Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
  • Collaborating with experts at study sites and with client representatives
  • Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices)
  • Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included

Qualifications:

  • University Degree in life science or other scientific discipline or apprenticeship in the health care field
  • Minimum of twoyears of on-site monitoring experience
  • Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment
  • Fluency in German on at least C1 level and a good command ofEnglish
  • Flexibility to travel up to 40-60% of working time
  • Driver’s license class B

What you can expect:

  • Resources that promote your career growth
  • Leaders that support flexible work schedules
  • Programs to help you build your therapeutic knowledge
  • Dynamic work environments that expose you to new experiences
  • Home-office, company car, accident insurance and more
  • Monthly gross salary: starting at 4.200 EUR basic - an overpay according to skills and working experience is possible

Whatever your career goals, we are here to ensure you get there!
Please apply with your English CV and motivation letter.
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 to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Originally posted on Himalayas

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