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主题: 猎头招聘:外资500强医药公司招聘Clinical Research Associate-上海
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作者 猎头招聘:外资500强医药公司招聘Clinical Research Associate-上海   
Joycepan





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加入时间: 2007/01/11
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文章标题: 猎头招聘:外资500强医药公司招聘Clinical Research Associate-上海 (1963 reads)      时间: 2009-11-10 周二, 16:40   

作者:Joycepan海归招聘 发贴, 来自【海归网】 http://www.haiguinet.com

JOB PURPOSE:
Sets up, monitors and reports on clinical trials in conformity with ICH / GCP, WWCD SOPs and local /regional regulation.


KEY ACCOUNTABILITIES:
1. Participates in the creation of clinical trial documents in collaboration with the clinical project leader.
2. Identifies and selects investigators in collaboration with the clinical project leader
3. Prepares / collects all documents needed prior to study initiation.
4. Performs / participates in study set up visits in the investigational centres (hospitals, CROs…) and organises / participates in study initiation meetings in which are provided scientific and technical knowledge concerning the study procedures and its organisation.
5. Ensures monitoring follow up:
 Relations and rendez-vous with the investigational centres.
 Follow up of trial progress and quality control of data (source document check).
 Documentation of protocol violations, adverse events and premature treatment cessation.
 Identification and resolution of all problems: logistical, methodological, human technical, which occur during a study.
 Management of the local trial files
 Management of the investigator’s trial file
 Management of trial related logistics
 Detection and reporting of deviations, finding and implementing corrective measures
6. Provides timely written documentation of all visits / contacts in appropriate reports.
7. Performs post study monitoring visits to close investigational centres.
8. Manages documents on a local level:
 CRFs and special forms
 DRFs
 Data entry into the monitoring tool.
 Mail, contact reports, monthly activity reports
9. Prepares, organises and participates in investigator’s meetings
10. Participates in internal & external education and training
11. Prepares and follows up investigational centres and system audits (QA)
12. Organises the trial filing and archiving

JOB-HOLDER ENTRY REQUIREMENTS:
Education:
master degree in clinical medicine or pharmacy

Experience & knowledge:
Previous experience in monitoring clinical trails is required

Core competencies:
Good command of English (written and spoken)
Knowledge of PC (WORD, EXCEL, POWERPOINT)
Interpersonal communication skill
Team player

有意者请联系:[email protected]

作者:Joycepan海归招聘 发贴, 来自【海归网】 http://www.haiguinet.com









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