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无工作经验 -
本科 -
招若干人 -
11-09 发布
- 五险一金
- 专业培训
- 补充医疗保险
- 定期体检
职位描述
职位描述： inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 7,000 employees in more than 36 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bio-analytical services, and strategic resourcing from a single clinical professional to an entire functional team.Location: Beijing or Shanghai Do you have the required skills? · Degree from a health care or scientific discipline, a nursing qualification preferred but not essential. · Relevant experience working as CTC, CTA or Administrative support acceptable. · Proven ability to work within a team and deliver on commitments. · Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements. · Ability to work independently in a fast-paced environment. · Strong communication, interpersonal, and organizational skills. · Must demonstrate good computer skills. Great Benefits with the role · Excellent team culture · Great leadership and ongoing support · Competitive remuneration and benefits package Responsibilities · Making arrangement for Investigator Meetings & Study Team Meetings including taking minutes. · Assist with the Ethics / Regulatory Submissions and keep a track of submissions & approvals for the study. · Preparing copies of Protocols, Investigator Brochures and CRFs which includes keeping track and re-ordering supplies. · Setting up and maintenance of the Trial Master Files (TMF) or Electronic filing systems/ set up of the Investigator Site File (IF) · Managing and maintaining study documents & trial supplies e.g.; Patient Information sheets, Patient Diaries, Lab Kits & Medical equipment for sites. · Preparing essential clinical trial documentation, distributing, tracking and filing of documents on return. · Create & maintain study contact lists for team/sites/3rd parties etc. · Sending out Study Newsletters / Study Correspondence to all participating sites on an ongoing basis · Setting up of finance systems accurately, processing invoices & tracking payments for the trial for investigator payments. · Assist with collating, tracking & shipping CRFs & data queries to Data Management. · General study filing, including uploading of documents into global repository. · Coordinating archival of study documentation. · Arranging translation of patient documents. · Assisting Clinical Research Associates on monitoring visits i.e. file reconciliation. · Re-ordering clinical drug supplies for sites, arranging for trial drug destructions with external vendors. We offer exciting opportunities, competitive packages, ongoing support, career development, training opportunities and flexible career options at leading global companies including the top biopharmaceutical MNCs to our employees. 职能类别： 临床研究员 临床协调员 关键字： CTA CTC Project Assistant 周末双休 带薪年假 奖金丰厚 节日福利 采暖补贴 话补
联系方式
国贸
公司信息
InVentiv Health通过分布在全球70多个国家的14000名员工，为医药、医疗器械和生物工程客户提供临床研发、销售及商务咨询服务，inVentiv Health的目标是通过自身的专业服务将客户的商业理念真正地转化为现实，帮助客户提升业绩，现在inVentiv Health服务于约550家客户的850个品牌。 2011年12月，inVentiv Health在中国设立盈帆达医药咨询（上海）有限公司，正式在中国区域为医药行业客户提供服务。 inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 7,000 employees in more than 36 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bio-analytical services, and strategic resourcing from a single clinical professional to an entire functional team.
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