
臨床數(shù)據(jù)監(jiān)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(yè)簡介
白鷺醫(yī)藥技術(shù)(上海)有限公司[Egret Pharma (Shanghai) Ltd.] 位于著名的上海“張江藥谷”,于2003年注冊(cè),是一家由美中醫(yī)藥界知名企業(yè)家、科學(xué)家團(tuán)隊(duì)創(chuàng)辦的美資企業(yè)。公司致力于創(chuàng)新藥物的研究和開發(fā),立志在中國打造出具有自主研發(fā)能力的國際化現(xiàn)代藥物企業(yè)。
公司創(chuàng)始人及管理團(tuán)隊(duì)來自國際醫(yī)藥界知名的企業(yè)家和學(xué)術(shù)科研精英。他們熟悉行業(yè)的國際市場(chǎng)運(yùn)行環(huán)境及運(yùn)行規(guī)則,并有成功創(chuàng)辦NASDAQ上市公司的經(jīng)驗(yàn)。管理團(tuán)隊(duì)成員(CEO,CSO,COO)在美國跨國制藥公司有10年以上藥物研發(fā)和管理經(jīng)歷,在新藥開發(fā)領(lǐng)域,如現(xiàn)代藥物化學(xué)、組合化學(xué)、藥物設(shè)計(jì)、ADME、動(dòng)物試驗(yàn)、臨床試驗(yàn)及研發(fā)管理等方面有獨(dú)特的技術(shù)優(yōu)勢(shì)。為確保公司的研發(fā)工作處于世界一流水平,公司還聘請(qǐng)歐美主流醫(yī)藥界之資深專家擔(dān)任公司的長期顧問。公司建立有符合國際一流標(biāo)準(zhǔn)的軟硬件系統(tǒng)及管理體系,擁有先進(jìn)的現(xiàn)代藥物研究設(shè)備和實(shí)驗(yàn)條件,以及一流的文獻(xiàn)檢索數(shù)據(jù)庫和信息管理系統(tǒng),并已全面實(shí)現(xiàn)科研工作信息的電子化管理。
目前,藥物的知識(shí)產(chǎn)權(quán)問題引起了中國政府乃至社會(huì)各界的廣泛關(guān)注,新藥創(chuàng)制領(lǐng)域有著廣闊的發(fā)展空間;公司以上海為立足點(diǎn),將市場(chǎng)目標(biāo)定位于整個(gè)中國市場(chǎng)及歐美主流市場(chǎng);加之公司的人才、技術(shù)優(yōu)勢(shì),以及開放、高效、和諧的人文環(huán)境;白鷺醫(yī)藥可謂“天時(shí)、地利、人和”。
職位發(fā)布企業(yè)

白鷺醫(yī)藥技術(shù)(上海)有限公司
企業(yè)性質(zhì):外資企業(yè)
企業(yè)規(guī)模:1-49人
成立年份:2003
企業(yè)地址:上海浦東新區(qū)張江高科哈雷路1118號(hào)4樓
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職位發(fā)布日期: 2016-03-24