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Biogen Idec
Sr Associate II, GMP Compliance
Massachusetts
11/20/2009 8:50 AM
As a key contributor within the Global GxP Compliance (GGC) organization, the individual will be primarily responsible for representing GGC and assuring compliance in numerous compliance teams. The individual will have the ability to effectively communicate compliance issues and expectations with Biogen Idec internal customers and management. The individual will have the ability to perform risk as
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Biogen Idec
Audit Project Manager
Massachusetts
11/13/2009 8:48 AM
Position Summary This position is the most senior level position in the internal audit staff. Assists in planning, managing and execution of high risk integrated financial, IT and operational audits of functions and affiliates worldwide in order to provide assurance to operating management that Corporate and Finance Policies and Procedures are complied with. Assist Internal Audit management in
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Biogen Idec
Clinical Trial Manager
Massachusetts
11/13/2009 8:48 AM
As a key member of the clinical operations team at Biogen Idec's Syntonix subsidiary, this individual will play a critical role in advancing our hemophilia programs on a global basis with the overall goal of significantly improving treatment options for patients and their families. Relying on a strong understanding of effective clinical trial management, this individual will translate program stra
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Biogen Idec
Clinical Program Leader
Massachusetts
11/13/2009 8:48 AM
As a key member of the clinical operations team at Biogen Idec's Syntonix subsidiary, this individual will play a critical role in advancing our hemophilia programs on a global basis with the overall goal of significantly improving treatment options for patients and their families. Relying on a strong understanding of effective clinical trial management, this individual translates program strategy
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Biogen Idec
VP, Regulatory Affairs Syntonix
Massachusetts
11/11/2009 7:44 AM
The Head of Regulatory Affairs for Syntonix will provide leadership, strategic direction and day-to-day oversight of global regulatory development and registration activities. He or she will play a pivotal role in devising and implementing innovative regulatory approaches that allow us to rapidly establish a global, market-leading hemophilia franchise and continue as a source of innovative product
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Biogen Idec
Senior Manager, Marketing - Tysabri
Massachusetts
11/10/2009 8:06 AM
Leads development and tactical execution of US marketing plans and programs in support of company/brand objectives of volume, market share, and profitability. Acts as liaison with internal and external partners to lead and guide brand tactics. May support/participate in large Commercial projects and initiatives. Responsibilities: Organize, lead and manage logistics and tactical execution
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Biogen Idec
Manager, Business Analysis
Massachusetts
10/30/2009 10:49 AM
HR Business partnership and technology expertise Serve as an IT liaison to the business through building, maintaining/fostering a partnership; expected to contribute to IT strategy, partner with IT leadership Demonstrate strong understanding of the overall HR business unit and supporting technology, with high-level understanding of how HR relates to other business units Project manage
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Biogen Idec
eDiscovery Operations Manager
Massachusetts
10/30/2009 10:49 AM
Responsibilities: eDiscovery technology strategy, implementation, and operations. To include all hardware and software systems related to the preservation and collection of Electronically Stored Information (ESI). Maintain the highest level of data quality control with respect to chain of custody on all matter related ESI. Remain current with best industry standard litigation support tech
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Biogen Idec
Manager, Regional Meeting Planning
Massachusetts
10/30/2009 10:49 AM
Develop, manage and motivate a team of 10 Regional Meeting Planners who are responsible for the execution and planning of all local and national Patient Empowerment Programs, local and national Peer to Peer Programs, Regional Sales Meetings, and Regional Training Meetings for the Neurology business unit. To manage the local and national Patient Empowerment Program & Peer to Peer projects fo
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Biogen Idec
Scientist I, Stability
North Carolina
10/30/2009 10:49 AM
Support operational and technical aspects of clinical drug substance, drug product, reference standard, and placebo GMP stability programs. Ensure compliance and support of company Standards, Practices, and SOPs as well as ICH and FDA guidelines. Provide technical expertise and leadership for the stability program of Cambridge-based commercial and clinical products. This includes design of stabili
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