更新于 11月24日

CRA(FSP)

1.1-1.4万
  • 上海徐汇区
  • 1-3年
  • 大专
  • 全职
  • 招2人

职位描述

医疗器械监查
In general, it provides site monitoring and
management services on DUA/RWE/PMS studies within MAO function and coordinate
the operational budget and resources across multiple tasks to ensure that studies
conduction meets performance targets and results.
- Arranging Site/Investigator Selection visit to assess
the eligibility of the site.
- Support on EC submission and approval before any
study activities.
- Acting as primary company contact for
assigned trial sites, engaging with Investigator and Site Staff throughout study
period. (Investigator meetings, site visits, study progress, issues/resolutions,
etc.).
- Proper training and communication to ensure
the study procedure and data collection requirement are well understood.
- Discussion of the recruitment plan and
study timeline with PI and site personnel to get alignment with targeted goal.
- Oversight of site study supplies and drugs/device/biologic
supplies to ensure the proper handling, storage and return with accurate
inventory and dispense records.
- ISF maintenance and ensuring secured
storage on site.
- Ensuring the data collection and query
resolution in a timely manner.
- Ensuring safety events are well documented
and timely reported per protocol requirement.
- Reporting of site progress
regularly and working with project leader on issues found on site in time and
providing updates until the issues are well resolved.
Metrics/KPIs: Metrics/KPIs governing these services are
based on the feedbacks from service- related stakeholders and project leaders.
Education and Experience Requirements:
· A minimum of a BA/BS degree, major in
Medicine/Nursing/Biomedicine are preferred.
· 1-2 years of relevant experience.
· Able to work effectively with all levels of the organization.
· Teamwork and collaboration
· Fluent in English reading and writing.
· Skillful at organizing and coordinating.
· Willingness to travel with overnight stay away from
home.
· Good time management skill.
· Good problem-solving skills and initiatives.
· Good computer skill (Word, Excel, Outlook, PowerPoint).
· Attention to detail.

工作地点

上海徐汇区亚太企业大楼

职位发布者

李经敏/HRD

昨日活跃
立即沟通
公司Logo君岳医药科技(上海)有限公司
君岳医药科技(上海)有限公司,是一家专研于器械科技(即医疗器械,体外诊断和AI科技)领域的临床研究服务机构(CRO)。从2015年成立,已经为多家国内外知名器械科技公司提供了专业的临床研究服务。公司提供的全方位临床研究服务范围覆盖从上市前研发,注册临床到上市后各个研究阶段,涵盖包括:临床监查、项目管理、医学事务、核心实验室、研究中心管理、生物统计、数据管理、注册事务、器械安全管理、医学翻译等服务,为客户提供器械科技研发的全生命周期一站式服务。公司核心管理团队均来自国际一线CRO公司和国际知名器械公司,拥有超过15年以上临床经验。他们能够为客户提供从临床研究的策略形成、运行实施、总结分析直至注册申报等全方位的专业服务,保证项目运营的最高效化,以及运营及研究风险的可控化。公司分别在心血管介入、神经介入、肿瘤、呼吸介入、人工智能、机器人、骨科、口腔、皮肤科等多治疗领域的注册研究和科研临床积累了丰富的经验,和临床研究中心及研究者保持着长期紧密的合作关系。同时,依托对于大中华区、欧美及亚太器械法规环境的熟悉了解,公司与各国当地监管机构积极合作,助力客户制定合理高效的注册策略,加速中国器械科技厂家的全球市场布局。公司网站:www.ccrcmed.com
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