广州招聘

岗位职责：

(a) Pre-trial Documentation 临床前文档的准备工作

(b) Trial Management: help investigator with trial management, including coordinating the submission of IRB/EC and Agreement signature process.试验管理：协助研究者进行试验管理，包括协调申报伦理、研究协议签署等。

(c) Support investigator’s daily work, including:协助研究者的日常工作，包括：

Labeling, packaging and storing all laboratory specimens before shipment to central lab.

Filling CRF under investigator’s approval.

(d) Subject Management:受试者管理：

Help investigator to identify and enroll potential study subjects.

Responsible for subjects’ follow-up, including visits arrangement, coordinating laboratory and obtaining results.

(e) Coordinating CRA’s routine visits.协调CRA 到site 的例行访视。

(f) Documents Management: Responsible for archiving and maintain trial related documents.临床试验档案管理：负责该中心的临床试验项目文件整理和归档。

(g) Drug Management: Including research drug accounting, receiving, saving, distributing and calling-back, and completing related record.协助完成临床研究药物管理和计数，包括药物的接收、保存、分发、回收和归还，并完成相关记录。

(h) Meeting Supporting: Provide logistic support for initiating meeting and any other investigator meeting.会议支持：负责各项启动会议、研究者会议的会务安排。

(i) Other daily work delegated by investigator.研究者指定的其它工作。

  Beijing Health Tech Medical Group (HT-Med) was founded since 2004. We are a comprehensive medical Operation and development organization .Assemble excellent talents of medicine, pharmacy, data management and statistical fields, offering professional services to support biotech and pharmaceutical companies at every stage of product lifecycle .
 
 We provide Medical translation, Data Management, Statistical Analysis, Medical Writing, Regulatory Affairs, Project Evaluation and Management, Independent Audit, Training, CRA/CRC/DM dispatch. Since we established, we were developing new drugs with Chinese Academy of Medical Sciences, Peking University Health Science Center, The General Hospital of the PLA, Military Medical Sciences, etc. Has cooperated with over 90% clinical trial sites (hospital) approved by SFDA.

  We developed independently EDC+CTMS by ourselves, obtained 3 patents and 2 brands. Basing on excellent IT capability, we develop Products Data Center for our clients, and created role exchange pattern between CRA and CRC, improved speed&quality of Clinical Study by the model of EDC+CRC, especially in PMS. We have been became the vendor of lots of global company (AZ, GSK, BI, Abbott, Roch, Mundipharma, QPS etc.) and some official Institution (Chinese Academy of Medical Sciences, Peking university, The general hospital of Chinese PLA, Sanming hospital, Zhejiang oncology hospital, Academy of Military Medical Sciences of the Chinese PLA etc.).

 We are familiar with China SFDA policy and CDE mentality, possessing mass of expert resource and marketing support. we could cover 90% Chinese certificated clinical research hospital by lots of home-based employee in 18 cities.

  公司网址：http://www.ht-med.com