经验丰富的临床研究专员，CRA (居家办公机会)
Experienced Clinical Research Associate, CRA (Home-Based opportunities
职位名称：经验丰富的临床研究助理，CRA（居家办公机会）
工作地点：远程，丹麦
工作地点类型：远程
工作合同类型：全职
职位级别：
我们的临床活动正在迅速增长，我们目前正在寻找全职、居家办公的临床研究助理加入我们在丹麦的临床运营团队（候选人可以位于丹麦任何地方）。该职位将与北欧团队合作，完成对公司成功至关重要的任务和项目。如果您希望从事一项充满挑战的职业，利用您以往的专业知识，并进一步发展和提升您的职业生涯，那么这就是您的机会。需要掌握当地语言并具备优秀的英语能力。
如果您正在寻找一家稳定、持续快速发展的CRO公司，Medpace是您的理想选择！我们目前正在寻找全职、居家或办公室办公的临床研究助理加入我们在丹麦充满活力的临床监查团队。我们提供一个可以进一步发展的职业机会，您可以运用现有的和以往的专业知识。
职责
- 对研究机构进行可行性、研究前、启动、监查和结题访问，主要涉及I至III期临床试验及所有可用治疗领域；
- 执行源文件验证和病例报告表审查；
- 执行法规文件审查；
- 进行研究药物库存管理；
- 执行不良事件和严重不良事件的报告和跟进；以及
- 评估患者招募和留存情况。
资格要求
- 生命科学相关领域的学士学位；
- 至少1.5年的独立监查经验；
- 熟悉医学术语和临床患者管理；
- 了解药物治疗技术和临床研究方法；
- 需掌握当地语言并具备优秀的英语能力。
Medpace简介
Medpace是一家全方位临床合同研究组织（CRO）。我们为生物技术、制药和医疗器械行业提供I至IV期临床开发服务。我们的使命是通过科学且严谨的方法加速安全有效的医疗疗法的全球开发。我们在肿瘤学、心脏病学、代谢疾病、内分泌学、中枢神经系统、抗病毒和抗感染等所有主要领域利用当地的监管和治疗专业知识。总部位于
查看英文原文
Job Title: Experienced Clinical Research Associate, CRA (Home-Based opportunities
Job Location: Remote, Denmark
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
Our clinical activities are growing rapidly, and we are currently seeking full-time, home-based Clinical Research Associates to join our Clinical Operations team in Denmark (candidates can be based anywhere in Denmark). This position will work on a Nordic team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Fluency in local language and excellent English are required.
If you are looking for a stable, consistently, rapidly, developing CRO, Medpace is a great place for you! We are currently seeking full-time, home or office-based Clinical Research Associates to join our energetic Clinical Monitoring team in the Denmark. We offer an exciting career where you can grow further, using your current and and previous expertise.
Responsibilities
- Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
- Perform source document verification and case report form review;
- Perform regulatory document review;
- Conduct study drug inventory;
- Perform adverse event and serious adverse event reporting and follow-up; and
- Assess patient recruitment and retention.
Qualifications
- Bachelor of Science in health-related field;
- Proven CRA experience of at least 1.5 years independent monitoring experience
- Broad knowledge of medical terminology and clinical patient management;
- Basic knowledge of drug therapy techniques and clinical research methodologies;
- Fluency in local language and excellent English are required.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 50+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Awards
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, 2024 and 2025
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Responsibilities
· Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
- Perform source document verification and case report form review;
- Perform regulatory document review;
- Conduct study drug inventory;
- Perform adverse event and serious adverse event reporting and follow-up; and
- Assess patient recruitment and retention.
Qualifications
· Bachelor of Science in health-related field;
- Proven CRA experience of at least 1.5 years independent monitoring experience
- Broad knowledge of medical terminology and clinical patient management;
- Basic knowledge of drug therapy techniques and clinical research methodologies;
- Fluency in local language and excellent English are required.
This job is curated by Lifelancer.
Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.
Please apply via Lifelancer platform to get connected to the application page and to find similar roles.
Originally posted on Himalayas