臨床數據監察員
職位描述
PRINCIPAL DUTIES AND RESPONSIBILITIES: Indicate key areas of responsibility, major job duties, special projects and key objectives for this position. These items should be evaluated throughout the year and included in the written annual evaluation.
The Clinical Data Supervisor will:
1. Analyze the enrollment status and alert the clinical program manager if unusual activities or absences of activities are detected
2. Verify accuracy of case report forms against study protocol
3. Monitor clinical data entry time and completeness based on scheduled clinical visits during a trial
4. Review laboratory data periodically and identify any laboratory values that are significantly outside the normal range.
5. Perform initial assessment to determine whether the abnormal values may result from a laboratory error or may be clinically significant and alert appropriate clinical project team members accordingly.
6. Review inclusion and exclusion criteria, medical history, demographics and or other baseline characteristics of study subjects to alert team to any eligibility violation
7. Review adverse event data and concomitant medication use to detect unusual or absent activities. Identify outliers in safety data pattern.
8. Review and revise adverse event and medication coding for consistency and accuracy
9. Perform periodic pharmacovigilance analysis to detect safety signals
10. Generate graphs and reports using spreadsheet and database tools
QUALIFICATIONS:
1. Bachelor of Medicine or related Life Science discipline, or higher
2. Completed courses in biochemistry and human physiology
SKILLS/ ABILITIES/ COMPETENCIES REQUIRED: (MUST be realistic, measurable, objective, and related to the essential functions of the job.)
1. Proficient in English reading and verbal communication
2. Proficient in Microsoft Excel and data table manipulations
3. Familiar with statistical methods for data analysis
4. Familiar with medical terms and laboratory testing principles
5. Familiar with database structure and electronic data capture is a plus
企業簡介
白鷺醫藥技術(上海)有限公司[Egret Pharma (Shanghai) Ltd.] 位于著名的上?!皬埥幑取?,于2003年注冊,是一家由美中醫藥界知名企業家、科學家團隊創辦的美資企業。公司致力于創新藥物的研究和開發,立志在中國打造出具有自主研發能力的國際化現代藥物企業。
公司創始人及管理團隊來自國際醫藥界知名的企業家和學術科研精英。他們熟悉行業的國際市場運行環境及運行規則,并有成功創辦NASDAQ上市公司的經驗。管理團隊成員(CEO,CSO,COO)在美國跨國制藥公司有10年以上藥物研發和管理經歷,在新藥開發領域,如現代藥物化學、組合化學、藥物設計、ADME、動物試驗、臨床試驗及研發管理等方面有獨特的技術優勢。為確保公司的研發工作處于世界一流水平,公司還聘請歐美主流醫藥界之資深專家擔任公司的長期顧問。公司建立有符合國際一流標準的軟硬件系統及管理體系,擁有先進的現代藥物研究設備和實驗條件,以及一流的文獻檢索數據庫和信息管理系統,并已全面實現科研工作信息的電子化管理。
目前,藥物的知識產權問題引起了中國政府乃至社會各界的廣泛關注,新藥創制領域有著廣闊的發展空間;公司以上海為立足點,將市場目標定位于整個中國市場及歐美主流市場;加之公司的人才、技術優勢,以及開放、高效、和諧的人文環境;白鷺醫藥可謂“天時、地利、人和”。
熱門區域招聘: 重慶 北京 上海 浙江 江蘇 廣東 山東 湖南 安徽 河北
上海招聘企業: 百進冠合(海南) 醫療科技有限公司 上海華茂藥業有限公司 上海信誼藥廠有限公司 上海強生制藥 歐姆龍健康醫療(中國)有限公司 青海瑞成藥業(集團)有限公司 上海交通大學醫學院附屬瑞金醫院 復旦大學附屬中山醫院 上海復星醫藥 上海醫藥集團
職位發布日期: 2016-03-24