出海雷达

临床运营实习生

Clinical Operations Intern

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Infotree Global Solutions
薪资未公开
工作地点Poland
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Intern
发布时间10 天前
数据来源Himalayas
前往 Himalayas 查看并投递 →
注意地域限制:该职位明确限定在 Poland 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。

你是否是热爱生命科学的学生,希望在临床试验快节奏的环境中获得实践经验?我们正在与一家致力于为严重疾病患者开发突破性、高影响力的疗法的创新型生物技术公司合作。我们的客户在全球范围内运营,将尖端科学研究与注重持续学习和创新的协作文化相结合。加入他们的临床团队,你将与经验丰富的专业人士一起工作,并直接为推进救命治疗做出贡献。

主要职责
在此职位中,你将发挥关键作用,协助临床试验管理专员(CTMAs)和临床研究专员(CRAs),确保试验运作顺畅。

  • 文档管理:跟踪试验文档,执行试验主文件(TMF)相关活动(上传、索引和质量验证),并确保符合监管标准。
  • 系统与数据录入:准确地在内部系统中录入和维护关键试验数据,并维护操作跟踪表。
  • 报告:准备操作报告和演示材料以支持临床试验更新。
  • 监测支持:协助临床研究专员(CRAs/监查员)完成日常行政和操作任务。

候选人要求

  • 教育背景:需为在校学生,优先考虑药学、生物技术、化学、物理或相关生命科学领域的学位攻读者。
  • 技术技能:熟练使用MS Office(Excel、PowerPoint),熟悉Canva等图形设计工具,并对AI工具有实际理解。
  • 语言能力:具备良好的英语能力(至少B2级别),以进行日常有效沟通。
  • 软技能:出色的组织能力,注重细节,积极主动,沟通清晰。

你能获得什么?

  • 在临床研究行业获得实践性的现实工作经验。
  • 从经验丰富的行业专家那里获得指导。
  • 灵活的工作环境,围绕你的大学日程安排(100%远程,每周30小时)

最初发布于喜马拉雅斯

查看英文原文

Are you a passionate Life Sciences student looking to gain hands-on experience in the fast-paced world of clinical trials? We are partnering with an innovative biotechnology company dedicated to developing groundbreaking, high-impact therapies for patients with severe medical conditions. Operating on a global scale, our client combines cutting-edge scientific research with a collaborative culture that values continuous learning and innovation. By joining their clinical team, you will work alongside experienced professionals and directly contribute to advancing life-saving treatments.
Key Responsibilities
In this role, you will play a crucial part in supporting Clinical Trial Management Associates (CTMAs) and Clinical Research Associates (CRAs) to keep trial operations running smoothly.

  • Documentation Management: Track trial documentation, conduct Trial Master File (TMF) activities (uploading, indexing, and quality verification), and ensure compliance with regulatory standards.
  • System & Data Entry: Accurately enter and maintain critical trial data across internal systems and maintain operational trackers.
  • Reporting: Prepare operational reports and presentation materials to support clinical trial updates.
  • Monitoring Support: Assist Clinical Research Associates (CRAs/monitors) with daily administrative and operational duties.

Candidate Profile

  • Education: Active student status required, preferably pursuing a degree in Pharmacy, Biotechnology, Chemistry, Physics, or related Life Sciences fields.
  • Technical Skills: Proficiency in MS Office (Excel, PowerPoint), familiarity with graphic design tools like Canva, and a practical understanding of AI tools.
  • Language Proficiency: Good command of English (minimum B2 level) for effective everyday communication.
  • Soft Skills: Excellent organizational abilities, strong attention to detail, proactive attitude, and clear communication skills.

What's in It for You?

  • Gain practical, real-world experience in the clinical research industry.
  • Mentorship from seasoned industry professionals.
  • Flexible working environment tailored around your university schedule (100% remote, 30 hours per week)

Originally posted on Himalayas

本页面信息整理自 Himalayas,版权归原发布方所有。职位可能随时关闭,投递请以原始页面为准。 本站只做信息聚合展示,不参与招聘流程,也不向求职者收取任何费用。

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