In-House Clinical Research Associate I (Serbia, Poland or Spain)
职位标题：内诊研究员 I （塞尔维亚，波兰或西班牙）工作地点：虚拟塞尔维利亚工作地址类型：远程工作合同类型：全日制工作资深级别：加入一个全球合约资源组织 (CRO),创新达到目的。在世界范围内的临床试验中，我们以共同承诺通过高质量的临床研究改善生活为动力。我们的团队有能力创造性思考，拥有权，并提供有意义的工作，帮助将改变生命的治疗带来世界各地的患者。随着全球4000多名专业人士的合作，我们培养了一个包容性的环境，在这种环境中，各种观点都得到了重视，增长也得到鼓励，每一个贡献都有影响。无论你是建立你的职业生涯还是带来多年的经验，你将有机会学习，发展和帮助塑造临床研究的未来。作为世界范围内内部临床研究员 I,你将发挥重要作用，支持成功开展帮助患者护理推进的临床研究。通过与临床试验管理人员，现场 CRAs,研究地点和跨功能团队密切合作，你将有助于确保研究按照良好临床实践 (GCP) 和适用的监管要求进行。在这个角色中，你将为整个研究生命周期中的站点管理活动做出贡献，从站点启动到关闭。你的工作将帮助维持学习质量，支持站点参与，并确保在时间上实现重要里程碑和成果。你将成为一个协作全球环境的一部分，其中细节关注，强烈沟通和对临床研究的热情可以产生意义上的影响。你将与全球各个时区的团队合作。你将做什么 ·支持网站创业活动，包括可行性问卷协调，保密协议收集和基本文件管理。·通过审查，跟踪和准备试验主档 (TMF) 的相关地址记录来保持精确和符合的研究文献。· 与现场 CRA 合作，支持调查员站点文件维护，TMF 调整和质量控制活动。·开展远程监测活动并提供优惠服务。
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Job Title: In-House Clinical Research Associate I (Serbia, Poland or Spain)
Job Location: Virtual Serbia
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world.
With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research.
Make an Impact as an In-House Clinical Research Associate I at Worldwide
As an In-House Clinical Research Associate I, you'll play an important role in supporting the successful delivery of clinical studies that help advance patient care. Working closely with Clinical Trial Managers, field CRAs, study sites, and cross-functional teams, you'll help ensure studies are conducted in compliance with Good Clinical Practice (GCP) and applicable regulatory requirements.
In this role, you'll contribute to site management activities across the study lifecycle, from site start-up through closeout. Your work will help maintain study quality, support site engagement, and ensure critical milestones and deliverables are achieved on time.
You'll be part of a collaborative global environment where attention to detail, strong communication, and a passion for clinical research can make a meaningful impact on study success.
Where You'll Work
This is a remote role open to candidates based in Serbia, Spain or Poland. You will collaborate with global teams across multiple time zones.
What You'll Do
- Support site start-up activities, including feasibility questionnaire coordination, confidentiality agreement collection, and essential document management.
- Maintain accurate and compliant study documentation by reviewing, tracking, and preparing site-related records for the Trial Master File (TMF).
- Partner with field CRAs to support Investigator Site File maintenance, TMF reconciliation, and quality control activities.
- Conduct remote monitoring activities and support pre-study, initiation, interim, and closeout visits under the guidance of the CRA or study leadership team.
- Build strong relationships with investigative sites through regular communication and ongoing study support.
- Review electronic data capture (EDC) systems, assist with query resolution, and help ensure timely and accurate study data entry.
- Generate reports, maintain study trackers, and provide operational updates to Clinical Trial Managers and project teams.
- Support site staff management activities, including training documentation, regulatory document collection, system access requests, and delegation tracking.
- Assist sites with patient prescreening, screening, recruitment activities, and subject eligibility review tracking where applicable.
What You'll Bring
- Bachelor's degree in a medical, biological, physical, health, pharmacy, or related scientific discipline preferred; or a combination of relevant education, training, and clinical research experience.
- Clinical research experience as a Study Coordinator, Clinical Trial Assistant, or in another relevant clinical research role.
- Basic understanding of clinical research principles, processes, and Good Clinical Practice (GCP) requirements.
- Knowledge of FDA and/or EU regulations, ICH Guidelines, local regulatory requirements, and clinical research standard operating procedures.
- Familiarity with electronic clinical systems such as EDC, eCRF, and IVRS platforms.
- Strong organisational, planning, time management, and interpersonal communication skills.
- Proficiency in Microsoft Office applications.
- Fluent in English and a native local language, with fluency in at least one of the following additional languages required: French, German, Italian, or Spanish.
Discover the Difference
We love knowing that someone is going to have a better life because of the work we do. Discover the Difference at Worldwide Clinical Trials. Explore additional opportunities on our careers page, visit , or connect with us onLinkedIn.
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