Displaying all 6 results
Ironwood Pharmaceuticals, Inc. - Cambridge, MA
Reportingto the Vice President, Regulatory Affairs, the Director of Regulatory Affairs is responsible for developing the overall regulatory strategy for NCE (new chemical entity) development programs in assigned therapeutic area, assuring that regulatory documents are in compliance with health authority regulations and interacting with US and international health authorities.
Posted Jun 05, 2013
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Application Deadline: None
Ironwood Pharmaceuticals, Inc. - Cambridge, MA
The Sales Operations Manager, Analytics position is a critical support role within the U.S. Sales Operations group reporting to the Sr. Director of U.S. Sales Operations. This team member will manage, report, and analyze critical sales force effectiveness metrics to effectively support commercial business decisions among the U.S. Commercial teams. These reports and analytics include but are...
Posted May 31, 2013
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Application Deadline: None
Ironwood Pharmaceuticals, Inc. - Cambridge, MA
The Sales Operations Manager, Resource Management position is a critical support role within the U.S. Sales Operations group reporting to the Sr. Director of U.S. Sales Operations. This team member will manage, support, and analyze numerous resources, processes, and systems to effectively support the U.S. Commercial teams. These resources, processes, and systems include but are not limited ...
Posted May 31, 2013
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Application Deadline: None
Ironwood Pharmaceuticals, Inc. - Cambridge, MA
This position requires a highly motivated, detail and service orientated individual to be responsible for managing the worldwide collaboration accounting at Ironwood. The Company's lead product was approved for marketing in the US and Europe in 2012. The product is being commercialized in the US by Ironwood and its collaboration partner, Forest Laboratories, and the parties share e...
Posted May 22, 2013
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Application Deadline: None
Ironwood Pharmaceuticals, Inc. - Cambridge, MA
Ironwood recognizes that clinical outcome assessments are critical for achieving product regulatory approvals, creating robust and differentiated product profiles, informing health economic assessments, and providing important information to patients and health care professionals for therapeutic decision-making. The Head of Outcome Measurement Study Endpoints will be responsible for leading...
Posted Mar 04, 2013
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Application Deadline: None
Ironwood Pharmaceuticals, Inc. - Cambridge, MA
Reporting to the Vice President, Regulatory Affairs, the Director of CMC Regulatory Affairs will be responsible for developing and implementing CMC regulatory strategies as well as coordinating all aspects of CMC regulatory submissions. This person will represent the function of CMC regulatory on project teams within Ironwood as well as serve as the regulatory CMC liaison with partners on d...
Posted Feb 13, 2013
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Application Deadline: None