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Manager - Data Management 5 {& }% O$ R3 D9 F& [
Post Date: 09/17/2004
4 z9 B6 B. p/ VLocation: Edmonton , AB
/ z9 ?+ d, g3 e3 uAssignment: Consulting
( q: j& B& p$ I- L) D, Q$ T# GPay Rate: Neg. Depending on experience 7 a) W4 J0 v8 M5 d" g' p" W5 E9 u9 ~
Start Date: 10/04/2004 4 a* i) T: o" L7 ?
Industry: Pharmaceutical
% q; B; w6 G" l: X RJob Order Number: 511-006622
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& ]* t! R' I! H4 {' @+ u4 g4 \Requirements: 0 A9 ]+ M* Z( s8 {) K& |2 ]+ p
Our client requires at least 5 years experience in a major pharmaceutical industry, CRO or health research in a data management role with at least 2 years in a management or team leader role. Familiarity with PC based Data Management Systems using Oracle based software and SQL and/or SAS programming skills are also mandatory. This position also requires excellent written and verbal skills with the ability to maintain a broad working knowledge of multiple on-going projects.
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Description: 8 ^0 M- q% ?+ `% }' q9 h) Q E
The Manager of Data Management, reporting to the Director, Information Systems, supervises the data management team involved in multiple clinical trials from a technical, methodological, training, and administrative standpoint. You will be acting as Principal Data Manager on new clinical trials. This position will interact with other managers in the Information Systems department and with the different BCIRG Clinical Operations teams in order to maintain the highest level of integrity through the process of data collection, entry, validation, and reporting for several ongoing breast cancer clinical trials. Key Responsibilities:- Manage a 10 person (and growing) Data Management team, which includes 5 Clinical Data Managers, 3 Clinical Data Co-Ordinators, 1 Programmer and 1 Coding Clerk.- Provide the team with the technical and methodological support related to the planning, implementation, and execution of all the data management and programming tasks assigned to each individual. - Supervise the execution of the data management and programming tasks (including Computerized System Validation) related to each clinical trial, constantly review the accomplishment of the pre-defined milestones, identify the issues, and put in place the appropriate corrective actions.- Contribute to the technical, methodological, and administrative homogenization within the team involved in different clinical trials, with the Director, Information Systems.- Contribute to plan for departmental needs including personnel training and resource utilization in collaboration with the Director, Information Systems.- Ensure an effective communication and collaboration within the team and between the team and other Clinical Operation teams (e.g., project management, drug safety, monitoring resources, and statistical department) to ensure needs are met.- Contribute to develop Standard Operating Processes and explore new technologies in collaboration with the Director, Information Systems.- Maintain awareness, utilize and conform to industry standards and regulatory requirements 1 b. z, ^4 j5 [9 U+ f" f
With more than 100 locations in North America, Europe, and Australia, Robert Half Technology is a leading provider of IT professionals on a project and full-time basis for IT initiatives ranging from Internet development and multiplatform systems integration to network engineering and technical support. Robert Half Technology offers online job search services at www.roberthalftechnology.com.
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5 D2 a) d- _$ S/ CRobert Half Technology is an Equal Opportunity Employer u+ w$ E5 m0 N/ F- ?" ]: A3 `
( U1 E. V8 g) _8 K8 ^: Q% ?7 wApply for this job now or contact our branch office for additional information: 7 c2 A4 O0 K( C! A( m: t4 h
, |7 H8 i3 w+ iRobert Half Technology Edmonton
7 B* Y7 F, o* F6 y8 n3 W, T10180 - 101 Street
# n6 O" u; Q* iSuite 1280 # F7 ^" Q' h7 h( A- J2 W n/ k% z
Edmonton, AB T5J 3S4 5 v6 g2 I+ k! Z9 ]+ H' W% o( s
Phone : 780 - 426 - 6642
1 g& j& b6 H N8 y) q, wFax : 780 - 423 - 1581 |
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