盖博医药（上海）有限公司临床数据审核员&临床数据经理

公司行业：制药/生物工程 公司性质：外资(欧美) 公司规模：少于50人
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临床数据审核员 Clinical Data Reviewer
9 M. u2 a0 Q- R3 \  L; o, r电子邮箱： shanghaihr@grs-cro.com
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发布日期： 2008-01-30 工作地点： 上海市 招聘人数： 1 工作年限： 二年以上

  v6 l) q1 V. M8 L外语要求： 英语 熟练 学  历： 本科   
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! R$ a% G6 H% x! x& K职位描述：
Responsibilities:
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( p; i5 [. G: z9 N0 h- Performs Clinical Data Validation and review medical data for completeness, accuracy and consistence.
- Generates data queries and data clarification form.
' f1 p/ O1 u/ L/ ]" j& Q- Ensures integrity of clinical data and updates database with resolved DCFs.
1 S+ ]- A% x! }+ ?8 x" d" i! p! V- Develops data management documents (Data Entry guidelines, CRF completion Instructions, Data Validation Guidelines, etc)
) J9 Y/ R4 z4 T1 a4 n' j0 E- Coordinates and collaborates with Data Reviewers and Data Managers at all locations of the corporate offices.

2 _4 D7 ?  t; L) }! ?3 `8 w" kRequirements:
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1 c; }: ?' s. S- Bachelor's degree in medical or healthcare-related science. MS or above welcomed.
0 M$ j- S$ N# b0 @; F- Training in Data Management and related disciplines preferred.
" g$ a# U( M. b, m/ H3 }+ r- Work experience in clinical data management preferred.
4 q: Q: [, g5 P" @  {. t) y0 ]) {- Involvement in clinical trials and good understanding of medical data.
1 I0 Q/ V; D7 N" l# o; V- Fluent in English, and strong communication and analytical skills.
- Familiar with Windows Environment and its applications (Word, Excel and PowerPoint).
- Working experience in hospitals welcomed.
- Clinical Monitoring (CRA/Monitor) experience preferred.
1 \, T2 a4 ]" Y# P3 `+ ^, I& j1 P- BS in Computer Science and/or experience with relational database systems and SQL query language preferred.


. c' O( n8 g) j) E临床数据经理 Clinical Data Manager
电子邮箱： shanghaihr@grs-cro.com
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/ X' L  D7 w9 ?( X; O发布日期： 2008-01-30 工作地点： 上海市 招聘人数： 1 工作年限： 二年以上
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外语要求： 英语 熟练 学  历： 本科   
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职位描述：
: R/ y1 Y! L( ^  nResponsibilities:

" [* h/ j) Q$ `& j1 S0 A) j- Develops data management manual documents (Data Entry guidelines, CRF completion Instructions, Data Validation Guidelines, etc)
- Represents data management at project team meetings and provides updates to project team on status of CDM tasks.
- Supervises, coaches and develops staff
- Communicates with project managers and project coordinators regarding project team and / or client issues.
& c: `& m% j1 ~- Assures that the data management needs of assigned projects are met, reporting all areas of concerns to the Manager of Data Management or Director of Data Management to assure timely and appropriate resolution of internal project team and/or client issues.
7 W" q9 \5 U4 J$ x+ k3 [6 g- Coordinates the review of clinical trial data. Perform Clinical Data Validation and review medical data for completeness, accuracy and consistence. Generate data queries and data clarification form.
- Ensures adherence to all timelines associated with data management.
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( J/ k) _5 z3 L# v  u8 H2 cRequirements:
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8 x" L/ B; B1 G5 Z6 D- Medical degree or in healthcare-related science. MS or above welcomed.
- At least two years working experience in clinical data management in a pharmaceutical company or CRO.
: ~* t5 K' V; ]& B7 U# y& ^- Training in Clinical Data Management and related disciplines preferred.
- Supervisory experience preferred.
- s# I2 V6 q' |; T6 A7 \8 L( u$ W- Good understanding of clinical trials and medical data.
$ X  P# l% l7 Q2 r4 l- Fluent in English, strong communication and analytical skills.
4 L! i- S+ W. @0 d5 D( e- Demonstrated team-building skills and the ability to work successfully in a team environment.
- Medical working experience in hospitals welcomed.
6 W7 q7 m8 j- e8 l- Good at typing and familiar with Windows Environment and its applications (Word, Excel and PowerPoint).
- Clinical Monitoring (CRA/Monitor) experience preferred
- BS in Computer Science and/or experience with relational database systems and SQL query language preferred
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0 E1 L" v) ]4 |( l1 r公司简介
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Global Medical Consulting Services (Shanghai) Co., Ltd. is a wholly owned subsidiary of US-based Global Research Services, LLC (GRS). GRS has offices also in Langenfeld, Germany, Warsaw, Poland, and Montreal, Canada. GRS is a leader in the management of clinical research programs for the pharmaceutical, biotech, and medical device communities. The company provides a full range of consulting and clinical trial management services that include protocol design, project management, data management, clinical site monitoring, biostatistical analysis, and medical report writing.
3 s  @: t! F5 D. @( D地  址： 黄浦区南京东路299号宏伊国际广场1201室
邮政编码： 200001
联 系 人： 薜小姐
电子邮箱： shanghaihr@grs-cro.com