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本帖最后由 医药猎头Jz 于 2015-4-15 13:47 编辑 3 e5 ^0 ?% N$ ^
) |" H: f, g% J( Y' F500强药企招聘,工作地点北京,待遇丰厚。欢迎医学、药学、临床、生物工程等相关背景的同学申请。要求国内名校毕业或海归,硕士优先。要求英语听说读写优秀。简历请投:junzhezhang@careerintlinc.com (备注:公卫人)
9 `9 e7 c4 c4 l9 x 另本人长期代表500强药企招募临床试验流程中的各职位,想看工作机会的朋友欢迎投来简历,注明意向。我会结合合适的机会向您推荐。
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职位要求、职责如下:
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F1 j9 Y$ L( ?0 _# V8 E0 v8 GKnowledge And Skills:
8 T, P8 \0 o1 [) B* ~Preferably experience in Clinical Data Management Systems
0 {( l0 c5 F% ] I3 |/ t6 Y• Understanding of database and programming concepts, database structures, file structures 3 I0 n e! f, j, d2 Z
• Preferably an understanding of programming/query languages 7 G% M+ U; ~: i) G# m$ ]# r+ ~. k
• Some basic knowledge of data coordination processes and the progress of a clinical study ' a$ ~$ K, w2 ]8 w, D
• Ability to acquire and apply new technical skills
, U% ?* i0 l6 I- f# \. H; [• Ability to understand and to follow client business policies, tools, SOPs, regulations and guidelines & B$ K7 F. [. D
• Ability to foster a good communication and collaboration within CDM and with clinical study teams . |( e ?0 x) N V/ `8 v$ @
• Demonstrates flexibility and works proactively 5 B- M* w" ?0 c0 D2 a! q, G
• Ability to follow ambitious timelines and implementation plans while paying attention to details % Z& E0 e: f+ ^8 @; ~* W6 {4 L- g/ A
• Sufficient competence in English to understand study documents and correspondence / \8 Q9 j" n# S2 }1 J5 ?; l+ w
" a8 `1 r# u8 r. p/ {+ eFormal Education And Experience preferred: 7 g p/ Y: m2 a& w* S3 O
Bachelor degree or equivalent, preferably in a life science or mathematics-related area (e.g. computer science, statistics), or, experience in Clinical Development and/or Clinical Data Management
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Responsibilities: ! Z+ y I+ R0 E4 w- o% \
1、Performs data cleaning tasks following standard processes (e.g., manages DRFs, including review, correct the database as required, performing quality checks). ) z/ m$ t* f& @# ]( j* `
- Monitors the progress of data cleaning activities and the quality of the data; gives regular feedback and status reports to the SDM. 5 I9 U/ a- y& v: e# c1 U) K; y- t
- Deputizes for the SDM, when appropriate; may liaise directly with internal and external partners. & _/ z! ]; T5 D( B& V
High quality database locked on time ! Z* E6 H& Z0 `$ d. b' d
2、Participates in the development of protocols, CRFs, Data Management Plan, (including the Data Validation Plan and Data Review Report) as per company standards; may be involved in the test of the edit checks.
: E2 N& _5 ?% B$ ~- a8 fHigh quality CRFs, Data Management Plan, including Data Validation Plan and Data Review Report ! \5 A& P$ n0 G4 \* Q L4 p
3、- Continually contributes to the evaluation of CDM processes for improvements. Best practices applied to all aspects of CDM study activities* f4 n5 D" }$ M$ K4 l
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