Trainee Clinical Research Associate (m/w/d), Home-Office throughout Germany

免费注册后解锁"你的匹配分 vs 高分画像"与个人技能缺口。

Why join Clinical Functional Service Partnerships (CFSP)? At IQVIA , our Clinical Functional Service Partnership (CFSP) model gives you the best of both worlds: the variety and sponsor-level exposure of working as an embedded member of a leading pharmaceutical or biotechnology team, backed by the stability, global infrastructure, and career support of IQVIA . You'll develop deep, specialist expertise on a dedicated program, with the flexibility to expand across sponsors and therapeutic areas as your career progresses - and the security of a long-term IQVIA career even as individual programs evolve. Through our long-standing partnerships with the world's leading pharmaceutical and biotechnology companies, you'll contribute to clinical research programs that bring innovative treatments to patients worldwide, working across all phases of development and a broad range of therapeutic areas, within a culture that supports flexibility, continuous learning, and wellbeing. About the role At IQVIA , you'll apply your clinical research expertise to drive meaningful outcomes for patients and sponsors around the world. As a Trainee Clinical Research Associate / Associate CRA (m/w/d) , you'll work across innovative studies and therapeutic areas, build your reputation with leading pharmaceutical and biotechnology partners, and grow your skills through structured training, mentorship, and genuine global career pathways. If you're ready to take ownership of site relationships, sharpen your expertise, and help bring life-changing treatments to patients worldwide, we'd love to hear from you. Key responsibilities Complete therapeutic area, protocol-specific, and clinical research training required to perform assigned responsibilities. Gain practical experience in study conduct and site management through collaboration with experienced clinical research professionals. Conduct site qualification, initiation, monitoring, and close-out visits in accordance with study protocols, GCP, ICH guidelines, and applicable regulatory requirements. Ensure investigational sites maintain high standards of patient safety, data integrity, protocol compliance, and study quality. Build and maintain effective relationships with investigators and site personnel, providing ongoing guidance, training, and support throughout the study lifecycle. Monitor study progress, including regulatory documentation, patient recruitment and enrollment, data query resolution, and site performance metrics. Collaborate with sites to implement and optimize patient recruitment and retention strategies to support study timelines. Maintain accurate, complete, and inspection-ready study documentation, including Investigator Site Files (ISF), Trial Master Files (TMF), monitoring reports, and follow-up communications. Identify, assess, and appropriately escalate study risks, site issues, and quality concerns while driving timely resolution. Partner closely with cross-functional study teams to support successful study execution and delivery of project objectives. What you’ll bring University degree in Life Sciences, Health Sciences, Nursing, Pharmacy, or a related discipline, or equivalent combination of education and experience. Completed advanced training in clinical research with 2-6 month duration is mandatory. Good knowledge of clinical trial processes, Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements. Excellent communication, organizational, and stakeholder management skills. Fluent written and verbal communication skills in German language (minimum C1 level) , along with a strong command of English. Ability to work independently, manage multiple priorities, and collaborate effectively within cross-functional teams. Willingness to travel within the assigned region (up to 40-60% of working time). A valid Class B driver's license. Home-office location throughout Germany (preference is North-Rhin-Westphalia, the Hamburg area, or the Frankfurt area). Availability to st

为什么加入临床职能服务合作伙伴关系（CFSP）？在IQVIA，我们的临床职能服务合作伙伴关系（CFSP）模式为您提供两全其美的体验：既能作为领先制药或生物技术团队的嵌入式成员，获得多样化的经验和申办方层面的曝光，又能享有IQVIA的稳定性、全球基础设施和职业支持。您将在专属项目中培养深入的专业知识，并随着职业发展灵活拓展至不同申办方和治疗领域——同时，即使个别项目发生变化，您也能拥有IQVIA长期职业发展的保障。通过我们与全球领先制药和生物技术公司的长期合作伙伴关系，您将为临床研究项目做出贡献，将创新疗法带给全球患者，工作涵盖各个开发阶段和广泛的治疗领域，并处于一个支持灵活性、持续学习和福祉的文化中。关于该职位在IQVIA，您将运用您的临床研究专业知识，为全球患者和申办方推动有意义的成果。作为培训生临床研究助理/助理CRA（m/w/d），您将在创新研究和治疗领域中工作，与领先的制药和生物技术合作伙伴建立声誉，并通过结构化培训、导师指导和真正的全球职业发展路径来提升技能。如果您准备好掌控研究中心关系、精进专业知识，并帮助将改变生命的疗法带给全球患者，我们期待您的加入。主要职责完成治疗领域、方案特定和临床研究培训，以履行分配职责。通过与经验丰富的临床研究专业人员合作，获得研究实施和研究中心管理的实践经验。根据研究方案、GCP、ICH指南和适用法规要求，进行研究中心的资格评估、启动、监查和关闭访问。确保研究研究中心在患者安全、数据完整性、方案合规性和研究质量方面保持高标准。与研究者 and 研究中心人员建立并维护有效关系，在整个研究生命周期中提供持续指导、培训和支持。监查研究进展，包括法规文件、患者招募和入组、数据质疑解决以及研究中心绩效指标。与研究中心合作实施和优化患者招募和保留策略，以支持研究时间线。维护准确、完整且可供检查的研究文档，包括研究者文件夹（ISF）、试验主文件（TMF）、监查报告和后续沟通记录。识别、评估并适当升级研究风险、研究中心问题和质量问题，同时推动及时解决。与跨职能研究团队紧密合作，支持研究成功执行和项目目标交付。您将带来生命科学、健康科学、护理学、药学或相关学科的大学学位，或同等教育和工作经验的组合。必须完成为期2-6个月的临床研究高级培训。良好的临床试验流程、良好临床实践（GCP）、ICH指南和法规要求知识。出色的沟通、组织和利益相关者管理能力。流利的德语书面和口头沟通能力（最低C1水平），以及较强的英语能力。能够独立工作、管理多项优先事项，并在跨职能团队中有效协作。愿意在指定区域内出差（最多占工作时间的40-60%）。有效的B类驾照。德国家庭办公地点（优先考虑北莱茵-威斯特法伦州、汉堡地区或法兰克福地区）。能够

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