临床研究助理 I
Clinical Research Associate I
我们是一家关注员工、客户、合作伙伴以及工作质量的公司。一家成立于1995年的充满活力的全球性企业，我们汇聚了3000多名积极进取、尽职尽责且充满热情的个人。我们在医学科学的最前线工作，改变人们的生活，为需要的人带来新的药物。
作为临床研究助理I，你将在与项目相关方沟通的一线工作，确保各种治疗领域的临床研究项目的进度、目标和标准。你将建立并维护与临床机构和研究人员的关系。你将专注于受试者的权利、安全和福祉以及数据合规性的质量。
你将：
· 进行并报告所有类型的现场监查访问
· 参与研究启动（如适用）
· 执行CRF审查、原始文件验证和问题解决
· 负责机构沟通和管理
· 作为内部支持服务和供应商的联系人
· 向内部项目团队汇报研究进展
· 参与可行性研究
· 协助监管团队准备研究提交文件
- 生命科学专业或同等教育、培训和经验组合的大学/本科及以上学历
- 临床研究或医疗经验
- 在英国具备独立现场监查经验
- 熟练使用MS Word、Excel和PowerPoint等办公软件
- 能够计划、多任务处理并在动态团队环境中工作
- 沟通、协作和解决问题的能力
- 能够出差
- 有效的驾驶执照
在一支知识渊博且专业的团队支持下，成为正式的临床研究专业人士。你将在公司中发展多种技能，并参与我们全面而具有挑战性的项目。
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We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
As a Clinical Research Associate I you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.
You will:
· Conduct and report all types of onsite monitoring visits
· Be involved in study startup (if applicable)
· Perform CRF review, source document verification and query resolution
· Be responsible for site communication and management
· Be a point of contact for in-house support services and vendors
· Communicate with internal project teams regarding study progress
· Participate in feasibility research
· Support regulatory team in preparing documents for study submissions
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Clinical Research or Medical experience
- Independent on-site monitoring experience in the UK
- PC skills to be able to work with MS Word, Excel and PowerPoint
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
- Valid driver’s license
Become a full-fledged clinical research professional with the support of a knowledgeable and professional team. You will develop a variety of skills while progressing with the company and contributing to our full-scale challenging projects.