天津招聘

职位描述：
Job Responsibilities:
? Prepare clinical trial required essential documents for regulatory submission or for investigator meeting, per request of project leader
? Prepare blank Trial Master File (TMF) and investigator file with index, per request of project leader
? Timely scan and e-file essential documents according to index provided by project leader during the conduct of the clinical trial
? Take responsible for essential documents transmittal during the conduct of the clinical trial, per request of project leader
? Compile paper-version and e-version essential documents for long term archiving according to related SOP. Assist in investigator file long term archiving in sites.
? Assist in logistics in project review meeting, project TC and VC
? Consolidate study progress report
? Make accrual according to study progress provided by project leader

Job Requirements:
? Research or health care related academic or work experience preferable.
? Good organizational skills, ability to manage multiple tasks and meticulous attention to detail.
? Good written and verbal communication skills.
? Good written and spoken English.
? Computer literacy: e.g. Microsoft Word, Excel, PowerPoint, Outlook.
? Have basic knowledge in GCP, SOP. 举报 分享

We are a global provider of consulting, and outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas. ICON has been recognised as one of the world’s leading Contract Research Organisations through a number of high-profile industry awards.